Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse

• Junko Matsuda

• Makiko Kido

• Keiko Tadano-Aritomi

• Ineo Ishizuka

• Kumiko Tominaga

• Kazunori Toida

• Eiji Takeda

• Kunihiko Suzuki

• Yasuhiro Kuroda

収録刊行物

• Human Molecular Genetics

  Human Molecular Genetics 13 (21), 2709-2723, 2004-09-02

  Oxford University Press (OUP)

キーワード

• Genetics (clinical)
• Genetics
• Molecular Biology
• General Medicine

詳細情報

• CRID: 1362544419941907200
• NII論文ID: 30018402937
• DOI: 10.1093/hmg/ddh281
• ISSN: 14602083
• ISSN: 09646906
• Web Site: http://academic.oup.com/hmg/article-pdf/13/21/2709/1582022/ddh281.pdf
• データソース種別:
  • Crossref
  • CiNii Articles