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Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in TRPV3 Gene.
Choi, Ji Young; Kim, Song Ee; Lee, Sang Eun; Kim, Soo Chan.
Afiliação
  • Choi JY; Department of Dermatology, Cutaneous Biology Research Institute, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
  • Kim SE; Department of Dermatology, Cutaneous Biology Research Institute, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
  • Lee SE; Department of Dermatology, Cutaneous Biology Research Institute, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
  • Kim SC; Department of Dermatology, Cutaneous Biology Research Institute, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea. kimsc@yuhs.ac.
Yonsei Med J ; 59(2): 341-344, 2018 Mar.
Article em En | MEDLINE | ID: mdl-29436206
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Mutação de Sentido Incorreto / Canais de Cátion TRPV Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans Idioma: En Revista: Yonsei Med J Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Mutação de Sentido Incorreto / Canais de Cátion TRPV Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans Idioma: En Revista: Yonsei Med J Ano de publicação: 2018 Tipo de documento: Article