<i>GJB1</i> Mutation-A Disease Spectrum: Report of Case Series.

GJB1 Mutation-A Disease Spectrum: Report of Case Series.

Niu, Jingwen; Dai, Yi; Liu, Mingsheng; Li, Yi; Ding, Qingyun; Guan, Yuzhou; Cui, Liying; Jin, Liri.

Afiliação

Niu J; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Dai Y; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Liu M; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Li Y; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Ding Q; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Guan Y; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Cui L; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Jin L; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.

Front Neurol ; 10: 1406, 2019.

Article em En | MEDLINE | ID: mdl-32010055

Palavras-chave

GJB1; X-linked Charcot-Marie-Tooth disease (CMTX1); case series; central nervous system; peripheral neuropathy; transient central nervous system symptoms

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article