Mutations of OCTN2, an Organic Cation/Carnitine Transporter, Lead to Deficient Cellular Carnitine Uptake in Primary Carnitine Deficiency

• N. L. S. Tang

• V. Ganapathy

• X. Wu

• J. Hui

• P. Seth

• P. M. P. Yuen

• T. F. Fok

• N. M. Hjelm

収録刊行物

• Human Molecular Genetics

  Human Molecular Genetics 8 (4), 655-660, 1999-04-01

  Oxford University Press (OUP)

キーワード

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

詳細情報

• CRID: 1363107370911865472
• NII論文ID: 30018400476
• DOI: 10.1093/hmg/8.4.655
• ISSN: 14602083
• ISSN: 09646906
• データソース種別:
  • Crossref
  • CiNii Articles