Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms

• B Klamt

収録刊行物

• Human Molecular Genetics

  Human Molecular Genetics 7 (4), 709-714, 1998-04-01

  Oxford University Press (OUP)

キーワード

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

詳細情報

• CRID: 1364233270525936640
• NII論文ID: 30018400792
• DOI: 10.1093/hmg/7.4.709
• ISSN: 14602083
• ISSN: http://id.crossref.org/issn/09646906
• Web Site: http://academic.oup.com/hmg/article-pdf/7/4/709/2675714/7-4-709.pdf
• データソース種別:
  • Crossref
  • CiNii Articles