Complete deletion of the aprataxin gene: ataxia with oculomotor apraxia type 1 with severe phenotype and cognitive deficit

詳細情報 詳細情報について

• CRID

  1360574094982159744

• DOI

  10.1136/jnnp.2007.127233

• ISSN

  00223050

• Web Site

  https://syndication.highwire.org/content/doi/10.1136/jnnp.2007.127233

• データソース種別

  • Crossref