Mutation analyses of patients with dyschromatosis symmetrica hereditaria: five novel mutations of the ADAR1 gene.

Liu, W; Wei, X-X; Liu, J-W; Habulieti, X; Yang, Z-Y; Qian, Y-T; Ma, D-L

Liu, W; Wei, X-X; Liu, J-W; Habulieti, X; Yang, Z-Y; Qian, Y-T; Ma, D-L.

Afiliação

Liu W; Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, National Clinical Research Center for Skin and Immune Diseases, Beijing, China.
Wei XX; Tianjin Medical Laboratory, BGI-Tianjin, BGI-Shenzhen, Tianjin, China.
Liu JW; Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, National Clinical Research Center for Skin and Immune Diseases, Beijing, China.
Habulieti X; Mckusick-Zhang Center for Genetic Medicine, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yang ZY; Tianjin Medical Laboratory, BGI-Tianjin, BGI-Shenzhen, Tianjin, China.
Qian YT; Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, National Clinical Research Center for Skin and Immune Diseases, Beijing, China.
Ma DL; Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, National Clinical Research Center for Skin and Immune Diseases, Beijing, China.

Clin Exp Dermatol ; 46(2): 347-348, 2021 Mar.

Article em En | MEDLINE | ID: mdl-32593192

Assuntos

Adenosina Desaminase/genética; Mutação; Transtornos da Pigmentação/congênito; Proteínas de Ligação a RNA/genética; Adolescente; Criança; Pré-Escolar; Feminino; Humanos; Masculino; Transtornos da Pigmentação/genética; Adulto Jovem

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos da Pigmentação / Adenosina Desaminase / Proteínas de Ligação a RNA / Mutação Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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