Literature DB >> 29923175

Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C-terminus of KIT.

T Takeichi1, K Sugiura2, K Tanahashi1, K Noda1, M Kono1, M Akiyama1.   

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Year:  2018        PMID： 29923175     DOI： 10.1111/bjd.16895

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  1 in total

1.  Case Report: A Missense Mutation of KIT in Hyperpigmentation and Lentigines Unassociated With Systemic Disorders: Report of a Chinese Pedigree and a Literature Review.

Authors:  Lu Yang; Yuehua Liu; Tao Wang
Journal:  Front Med (Lausanne)       Date:  2022-05-25
  1 in total

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