Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations

• Sanae Numata

• Yoshiro Koda

• Kenji Ihara

書誌事項

タイトル別名

• Mutant alleles associated with late onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations

抄録

コレクション : 国立国会図書館デジタルコレクション > デジタル化資料 > 雑誌

収録刊行物

• Journal of human genetics / Japan Society of Human Genetics

  Journal of human genetics / Japan Society of Human Genetics 55 (1), 18-22, 2010-01

  Tokyo : Springer Nature

キーワード

• haplotype
• late-onset
• male
• ornithine transcarbamylase deficiency
• recurrent mutation
• single nucleotide polymorphism

詳細情報

• CRID: 1520854805900752512
• NII論文ID: 10030733102
• NII書誌ID: AA11206160
• ISSN: 14345161
• NDL書誌ID: 10515382
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I10515382
• Web Site: https://search.jamas.or.jp/link/ui/2010209459
• 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