Identification of a Rare Novel KMT2C Mutation That Presents with Schizophrenia in a Multiplex Family.

Chen, Chia-Hsiang; Huang, Ailing; Huang, Yu-Shu; Fang, Ting-Hsuan

Chen, Chia-Hsiang; Huang, Ailing; Huang, Yu-Shu; Fang, Ting-Hsuan.

Afiliação

Chen CH; Department of Psychiatry, Chang Gung Memorial Hospital-Linkou, Taoyuan 333, Taiwan.
Huang A; Department and Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan.
Huang YS; Department of Psychiatry, Yuli Branch, Taipei Veterans General Hospital, Hualien 981, Taiwan.
Fang TH; Department of Psychiatry, Chang Gung Memorial Hospital-Linkou, Taoyuan 333, Taiwan.

J Pers Med ; 11(12)2021 Nov 25.

Article em En | MEDLINE | ID: mdl-34945726

Palavras-chave

KMT2C; histone 3 lysine 4; methylation; rare mutation; schizophrenia; whole-genome sequencing

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: J Pers Med Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Taiwan

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