Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome.

Oh, Seung Joon; Kim, Song-Ee; Lee, Sang Eun; Kim, Soo-Chan

Oh, Seung Joon; Kim, Song-Ee; Lee, Sang Eun; Kim, Soo-Chan.

Afiliação

Oh SJ; Department of Dermatology and Cutaneous Biology Research Institute, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Kim SE; Department of Dermatology and Cutaneous Biology Research Institute, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Lee SE; Department of Dermatology and Cutaneous Biology Research Institute, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Kim SC; Department of Dermatology and Cutaneous Biology Research Institute, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.

Ann Dermatol ; 28(4): 503-5, 2016 Aug.

Article em En | MEDLINE | ID: mdl-27489438

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Ann Dermatol Ano de publicação: 2016 Tipo de documento: Article