Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases, and a literature review in mainland Chinese patients

• Min Zhu

• Xuan Zhu

• Xueliang Qi

収録刊行物

• Journal of human genetics / Japan Society of Human Genetics

  Journal of human genetics / Japan Society of Human Genetics 59 (5), 256-261, 2014-05

  Tokyo : Springer Nature

キーワード

• electron transfer flavoprotein dehydrogenase
• genetic mutation
• hot spot mutation
• multiple Acyl-CoA dehydrogenation deficiency
• riboflavin

詳細情報

• CRID: 1520573330426806528
• NII論文ID: 40020066494
• NII書誌ID: AA11206160
• ISSN: 14345161
• NDL書誌ID: 025463176
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I025463176
• Web Site: https://search.jamas.or.jp/link/ui/2015132687
• 本文言語コード: en
• NDL 雑誌分類:
  • ZS16(科学技術--医学--人類遺伝学)
• データソース種別:
  • NDL
  • CiNii Articles