Clinical characteristics and molecular genetic analysis of 73 cases of tuberous sclerosis complex caused by TSC1/2 gene mutations in children.

Saved in:
Bibliographic Details
Title: Clinical characteristics and molecular genetic analysis of 73 cases of tuberous sclerosis complex caused by TSC1/2 gene mutations in children.
Authors: Wu X; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., He MY; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Xu HF; Department of Pediatrics, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China., He Y; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Min XH; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Zhao QK; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Liang SQ; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Ginowree NBN; Nanjing Medical University, Nanjing, Jiangsu, China., Hu SH; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Yin J; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Fan ZH; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Din MJU; Nanjing Medical University, Nanjing, Jiangsu, China., Zhu M; Department of Rehabilitation Medicine, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China., Zhang G; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Source: Frontiers in pediatrics [Front Pediatr] 2026 Apr 13; Vol. 14, pp. 1795318. Date of Electronic Publication: 2026 Apr 13 (Print Publication: 2026).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Media SA Country of Publication: Switzerland NLM ID: 101615492 Publication Model: eCollection Cited Medium: Print ISSN: 2296-2360 (Print) Linking ISSN: 22962360 NLM ISO Abbreviation: Front Pediatr Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 42051945
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Clinical characteristics and molecular genetic analysis of 73 cases of tuberous sclerosis complex caused by TSC1/2 gene mutations in children.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Wu+X%22">Wu X</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22He+MY%22">He MY</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Xu+HF%22">Xu HF</searchLink>; Department of Pediatrics, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.<br /><searchLink fieldCode="AU" term="%22He+Y%22">He Y</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Min+XH%22">Min XH</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Zhao+QK%22">Zhao QK</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Liang+SQ%22">Liang SQ</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Ginowree+NBN%22">Ginowree NBN</searchLink>; Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Hu+SH%22">Hu SH</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Yin+J%22">Yin J</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Fan+ZH%22">Fan ZH</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Din+MJU%22">Din MJU</searchLink>; Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Zhu+M%22">Zhu M</searchLink>; Department of Rehabilitation Medicine, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.<br /><searchLink fieldCode="AU" term="%22Zhang+G%22">Zhang G</searchLink>; Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101615492%22">Frontiers in pediatrics</searchLink> [Front Pediatr] 2026 Apr 13; Vol. 14, pp. 1795318. <i>Date of Electronic Publication: </i>2026 Apr 13 (<i>Print Publication: </i>2026).
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Media+SA%22">Frontiers Media SA </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101615492 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>2296-2360 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2222962360%22">22962360 </searchLink><i>NLM ISO Abbreviation: </i>Front Pediatr <i>Subsets: </i>PubMed not MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=42051945
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.3389/fped.2026.1795318
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 1795318
    Titles:
      – TitleFull: Clinical characteristics and molecular genetic analysis of 73 cases of tuberous sclerosis complex caused by TSC1/2 gene mutations in children.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Wu X
      – PersonEntity:
          Name:
            NameFull: He MY
      – PersonEntity:
          Name:
            NameFull: Xu HF
      – PersonEntity:
          Name:
            NameFull: He Y
      – PersonEntity:
          Name:
            NameFull: Min XH
      – PersonEntity:
          Name:
            NameFull: Zhao QK
      – PersonEntity:
          Name:
            NameFull: Liang SQ
      – PersonEntity:
          Name:
            NameFull: Ginowree NBN
      – PersonEntity:
          Name:
            NameFull: Hu SH
      – PersonEntity:
          Name:
            NameFull: Yin J
      – PersonEntity:
          Name:
            NameFull: Fan ZH
      – PersonEntity:
          Name:
            NameFull: Din MJU
      – PersonEntity:
          Name:
            NameFull: Zhu M
      – PersonEntity:
          Name:
            NameFull: Zhang G
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 13
              M: 04
              Text: 2026 Apr 13
              Type: published
              Y: 2026
          Identifiers:
            – Type: issn-print
              Value: 2296-2360
          Numbering:
            – Type: volume
              Value: 14
          Titles:
            – TitleFull: Frontiers in pediatrics
              Type: main
ResultId 1