Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutation

• Alison Fedyna

• Dennis Drayna

• Changsoo Kang

書誌事項

タイトル別名

• Characterization of a mutation commonly associated with persistent stuttering evidence for a founder mutation

収録刊行物

• Journal of human genetics / Japan Society of Human Genetics

  Journal of human genetics / Japan Society of Human Genetics 56 (1), 80-82, 2011-01

  Tokyo : Springer Nature

キーワード

• founder
• GNPTAB
• haplotype
• lysosome
• mucolipidosis
• stuttering

詳細情報

• CRID: 1524232505223134208
• NII論文ID: 10030657544
• NII書誌ID: AA11206160
• ISSN: 14345161
• NDL書誌ID: 10942750
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I10942750
• Web Site: https://search.jamas.or.jp/link/ui/2011270873
• 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