View in EDS PDF Full Text

Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening.

Saved in:
Bibliographic Details
Title: Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening.
Authors: Lin, Yiming1 (AUTHOR), Wang, Wenjun2 (AUTHOR), Lin, Chunmei1 (AUTHOR), Zheng, Zhenzhu1 (AUTHOR), Fu, Qingliu1 (AUTHOR), Peng, Weilin1 (AUTHOR) wellpeng@163.com, Chen, Dongmei3 (AUTHOR) chendm9090@163.com
Source: Orphanet Journal of Rare Diseases. 8/3/2021, Vol. 16 Issue 1, p1-8. 8p.
Database: Academic Search Ultimate
FullText Links:
  – Type: pdflink
Text:
  Availability: 0
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 151720101
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Lin%2C+Yiming%22">Lin, Yiming</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Wenjun%22">Wang, Wenjun</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lin%2C+Chunmei%22">Lin, Chunmei</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zheng%2C+Zhenzhu%22">Zheng, Zhenzhu</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fu%2C+Qingliu%22">Fu, Qingliu</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Peng%2C+Weilin%22">Peng, Weilin</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> wellpeng@163.com</i><br /><searchLink fieldCode="AR" term="%22Chen%2C+Dongmei%22">Chen, Dongmei</searchLink><relatesTo>3</relatesTo> (AUTHOR)<i> chendm9090@163.com</i>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 8/3/2021, Vol. 16 Issue 1, p1-8. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=151720101
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1186/s13023-021-01964-5
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 8
        StartPage: 1
    Titles:
      – TitleFull: Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Lin, Yiming
      – PersonEntity:
          Name:
            NameFull: Wang, Wenjun
      – PersonEntity:
          Name:
            NameFull: Lin, Chunmei
      – PersonEntity:
          Name:
            NameFull: Zheng, Zhenzhu
      – PersonEntity:
          Name:
            NameFull: Fu, Qingliu
      – PersonEntity:
          Name:
            NameFull: Peng, Weilin
      – PersonEntity:
          Name:
            NameFull: Chen, Dongmei
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 03
              M: 08
              Text: 8/3/2021
              Type: published
              Y: 2021
          Identifiers:
            – Type: issn-print
              Value: 17501172
          Numbering:
            – Type: volume
              Value: 16
            – Type: issue
              Value: 1
          Titles:
            – TitleFull: Orphanet Journal of Rare Diseases
              Type: main
ResultId 1