Haploinsufficiency of MITF is a Cause of Waardenburg Syndrome Type 2A(WS2A)
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概要
- 論文の詳細を見る
- 1996-08-01
著者
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TACHIBANA M.
Saitama Cancer Center Research Institute
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TAKEDA K.
Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders
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WATANABE A.
Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders
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NOBUKUNI Y.
Clinical Neurogenetics Branch, National Institute of Mental Health, NIH
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TACHIBANA M.
Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders
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SKARKA H.
Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders,
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Skarka H.
Laboratory Of Molecular Genetics National Institute On Deafness And Other Communication Disorders Ni
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NOBUKUNI Y.
Clinical Neurogenetics Branch, National Institute of Mental Health
関連論文
- C-02 Epistatic Relationship between Waardenburg Syndrome Genes MITF and PAX3.
- Interaction of MITF and a Ubiquitin-Conjugating Enzyme as Detected by the Yeast Two Hybrid System
- N- and C-terminal Regions are Required for MITF to Transactivate Tyrosinase Promoter
- Haploinsufficiency of MITF is a Cause of Waardenburg Syndrome Type 2A(WS2A)