Haploinsufficiency of MITF is a Cause of Waardenburg Syndrome Type 2A(WS2A)

この論文をさがす

著者

    • NOBUKUNI Y.
    • Clinical Neurogenetics Branch, National Institute of Mental Health
    • WATANABE A.
    • Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, NIH
    • TAKEDA K.
    • Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, NIH
    • SKARKA H.
    • Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, NIH
    • TACHIBANA M.
    • Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, NIH

収録刊行物

  • 日本分子生物学会年会プログラム・講演要旨集  

    日本分子生物学会年会プログラム・講演要旨集 19, 601, 1996-08-01 

各種コード

  • NII論文ID(NAID)
    10002916709
  • NII書誌ID(NCID)
    AN10468414
  • 本文言語コード
    ENG
  • 資料種別
    OTR
  • データ提供元
    CJP書誌 
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