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Entire PTCH1 deletion is a common event in point mutation-negative cases with nevoid basal cell carcinoma syndrome in Japan

CLINICAL GENETICS (2011)

Journal

CLINICAL GENETICS

Volume 79, Issue 2, Pages 196-198

Publisher

WILEY-BLACKWELL

DOI: 10.1111/j.1399-0004.2010.01527.x

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Ministry of Health, Labor and Welfare, Japan [H22-120]
Ministry of Education, Culture, Sports, Science and Technology, Japan [21591313]
Grants-in-Aid for Scientific Research [21591313, 23501269] Funding Source: KAKEN

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Entire PTCH1 deletion is a common event in point mutation-negative cases with nevoid basal cell carcinoma syndrome in Japan

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CLINICAL GENETICS

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WILEY-BLACKWELL

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Entire PTCH1 deletion is a common event in point mutation-negative cases with nevoid basal cell carcinoma syndrome in Japan

Journal

CLINICAL GENETICS

Publisher

WILEY-BLACKWELL

Keywords

Categories

Funding

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