[A novel mutation of SCN4A gene causes hypokalemic periodic paralysis in a Chinese family].

Li, H Y; Zhou, X L; Guo, J F; Tang, B S; Fu, Y J; Sun, J Y

Li, H Y; Zhou, X L; Guo, J F; Tang, B S; Fu, Y J; Sun, J Y.

Li HY; Department of Neurology, the People's Hospital of Anyang City, Anyang 455000, China.
Zhou XL; Department of Neurology, the People's Hospital of Anyang City, Anyang 455000, China.
Guo JF; Department of Neurology, Xiangya Hospitial, Central South University, Changsha 410008, China.
Tang BS; Department of Neurology, Xiangya Hospitial, Central South University, Changsha 410008, China.
Fu YJ; Department of Neurology, the People's Hospital of Anyang City, Anyang 455000, China.
Sun JY; Department of Neurology, the People's Hospital of Anyang City, Anyang 455000, China.

Zhonghua Yi Xue Za Zhi ; 100(45): 3622-3625, 2020 Dec 08.

Article en Zh | MEDLINE | ID: mdl-33333687

Asunto(s)

Parálisis Periódica Hipopotasémica; Adulto; Pueblo Asiatico/genética; Humanos; Parálisis Periódica Hipopotasémica/genética; Masculino; Mutación; Canal de Sodio Activado por Voltaje NAV1.4/genética; Linaje; Adulto Joven

Palabras clave

Hypokalemic periodic paralysis; Mutation; SCN4A gene; Vomit

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Parálisis Periódica Hipopotasémica Tipo de estudio: Etiology_studies / Screening_studies Límite: Adult / Humans / Male Idioma: Zh Año: 2020 Tipo del documento: Article

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