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

Center for Medical Genetics

Research output: Contribution to journal › Letter › peer-review

33 Citations (Scopus)

Original language	English
Pages (from-to)	93-95
Number of pages	3
Journal	Clinical Genetics
Volume	74
Issue number	1
DOIs	https://doi.org/10.1111/j.1399-0004.2008.01010.x
Publication status	Published - 2008 Jul

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1111/j.1399-0004.2008.01010.x

Cite this

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title = "Tietz syndrome: Unique phenotype specific to mutations of MITF nuclear localization signal",

author = "T. Izumi and A. Kohta and Y. Kimura and S. Ishida and T. Takahashi and A. Ishiko and Kenjiro Kosaki",

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TY - JOUR

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T2 - Unique phenotype specific to mutations of MITF nuclear localization signal

AU - Izumi, T.

AU - Kohta, A.

AU - Kimura, Y.

AU - Ishida, S.

AU - Takahashi, T.

AU - Ishiko, A.

AU - Kosaki, Kenjiro

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DO - 10.1111/j.1399-0004.2008.01010.x

M3 - Letter

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AN - SCOPUS:45149113805

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JO - Clinical Genetics

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

ASJC Scopus subject areas

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