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Article

Identification of a recurrent mitochondrial mutation in a Japanese family with palmoplantar keratoderma, nail dystrophy, and deafness.

European journal of dermatology : EJD - 1 Jan 2000

Hayashi Ryota, Fujiwara Hiroshi, Morishita Michiko, Ito Masaaki, Shimomura Yutaka

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 25513986
DOI: 10.1684/ejd.2014.2461

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