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Identification of a recurrent mitochondrial mutation in a Japanese family with palmoplantar keratoderma, nail dystrophy, and deafness.
Eur J Dermatol. 2015 Jan-Feb;25(1):79-81
Authors: Hayashi R, Fujiwara H, Morishita M, Ito M, Shimomura Y
PMID: 25513986 [PubMed - indexed for MEDLINE]
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