Tietz syndrome: Unique phenotype specific to mutations of MITF nuclear localization signal

T. Izumi; A. Kohta; Y. Kimura; S. Ishida; T. Takahashi; A. Ishiko; Kenjiro Kosaki

doi:10.1111/j.1399-0004.2008.01010.x

Tietz syndrome: Unique phenotype specific to mutations of MITF nuclear localization signal

T. Izumi, A. Kohta, Y. Kimura, S. Ishida, T. Takahashi, A. Ishiko, Kenjiro Kosaki

研究成果: Letter › 査読

本文言語	English
ページ（範囲）	93-95
ページ数	3
ジャーナル	Clinical Genetics
巻	74
号	1
DOI	https://doi.org/10.1111/j.1399-0004.2008.01010.x
出版ステータス	Published - 2008 7 1

ASJC Scopus subject areas

遺伝学
遺伝学（臨床）

文献へのアクセス

10.1111/j.1399-0004.2008.01010.x

他のファイルとリンク

引用スタイル

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AU - Takahashi, T.

AU - Ishiko, A.

AU - Kosaki, Kenjiro

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