View in EDS PDF Full Text

A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation.

Saved in:
Bibliographic Details
Title: A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation.
Authors: Kunii, Misako1, Doi, Hiroshi1, Higashiyama, Yuichi1, Kugimoto, Chiharu1, Ueda, Naohisa1, Hirata, Junichi1, Tomita-Katsumoto, Atsuko1, Kashikura-Kojima, Mari1, Kubota, Shun1, Taniguchi, Midori2, Murayama, Kei2, Nakashima, Mitsuko3, Tsurusaki, Yoshinori3, Miyake, Noriko3, Saitsu, Hirotomo3, Matsumoto, Naomichi3, Tanaka, Fumiaki1
Source: Journal of Human Genetics. Apr2015, Vol. 60 Issue 4, p187-191. 5p.
Database: Academic Search Ultimate
FullText Links:
  – Type: pdflink
Text:
  Availability: 0
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 102324534
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Kunii%2C+Misako%22">Kunii, Misako</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Doi%2C+Hiroshi%22">Doi, Hiroshi</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Higashiyama%2C+Yuichi%22">Higashiyama, Yuichi</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Kugimoto%2C+Chiharu%22">Kugimoto, Chiharu</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Ueda%2C+Naohisa%22">Ueda, Naohisa</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Hirata%2C+Junichi%22">Hirata, Junichi</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Tomita-Katsumoto%2C+Atsuko%22">Tomita-Katsumoto, Atsuko</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Kashikura-Kojima%2C+Mari%22">Kashikura-Kojima, Mari</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Kubota%2C+Shun%22">Kubota, Shun</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Taniguchi%2C+Midori%22">Taniguchi, Midori</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Murayama%2C+Kei%22">Murayama, Kei</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Nakashima%2C+Mitsuko%22">Nakashima, Mitsuko</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Tsurusaki%2C+Yoshinori%22">Tsurusaki, Yoshinori</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Miyake%2C+Noriko%22">Miyake, Noriko</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Saitsu%2C+Hirotomo%22">Saitsu, Hirotomo</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Matsumoto%2C+Naomichi%22">Matsumoto, Naomichi</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Tanaka%2C+Fumiaki%22">Tanaka, Fumiaki</searchLink><relatesTo>1</relatesTo>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Journal+of+Human+Genetics%22">Journal of Human Genetics</searchLink>. Apr2015, Vol. 60 Issue 4, p187-191. 5p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=102324534
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1038/jhg.2015.7
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 5
        StartPage: 187
    Titles:
      – TitleFull: A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Kunii, Misako
      – PersonEntity:
          Name:
            NameFull: Doi, Hiroshi
      – PersonEntity:
          Name:
            NameFull: Higashiyama, Yuichi
      – PersonEntity:
          Name:
            NameFull: Kugimoto, Chiharu
      – PersonEntity:
          Name:
            NameFull: Ueda, Naohisa
      – PersonEntity:
          Name:
            NameFull: Hirata, Junichi
      – PersonEntity:
          Name:
            NameFull: Tomita-Katsumoto, Atsuko
      – PersonEntity:
          Name:
            NameFull: Kashikura-Kojima, Mari
      – PersonEntity:
          Name:
            NameFull: Kubota, Shun
      – PersonEntity:
          Name:
            NameFull: Taniguchi, Midori
      – PersonEntity:
          Name:
            NameFull: Murayama, Kei
      – PersonEntity:
          Name:
            NameFull: Nakashima, Mitsuko
      – PersonEntity:
          Name:
            NameFull: Tsurusaki, Yoshinori
      – PersonEntity:
          Name:
            NameFull: Miyake, Noriko
      – PersonEntity:
          Name:
            NameFull: Saitsu, Hirotomo
      – PersonEntity:
          Name:
            NameFull: Matsumoto, Naomichi
      – PersonEntity:
          Name:
            NameFull: Tanaka, Fumiaki
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 04
              Text: Apr2015
              Type: published
              Y: 2015
          Identifiers:
            – Type: issn-print
              Value: 14345161
          Numbering:
            – Type: volume
              Value: 60
            – Type: issue
              Value: 4
          Titles:
            – TitleFull: Journal of Human Genetics
              Type: main
ResultId 1