CHRNE compound heterozygous mutations in congenital myasthenic syndrome: A case report.

Yang, Kunfang; Cheng, Hongyi; Yuan, Fang; Meng, Linyi; Yin, Rongrong; Zhang, Yuanfeng; Wang, Simei; Wang, Chunmei; Lu, Yanfen; Xi, Jiaming; Lu, Qin; Chen, Yucai

Yang, Kunfang; Cheng, Hongyi; Yuan, Fang; Meng, Linyi; Yin, Rongrong; Zhang, Yuanfeng; Wang, Simei; Wang, Chunmei; Lu, Yanfen; Xi, Jiaming; Lu, Qin; Chen, Yucai.

Afiliación

Yang K; Department of Neurology.
Cheng H; Department of Neurology.
Yuan F; Department of Neurology.
Meng L; Department of Pharmacy, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Yin R; Department of Neurology.
Zhang Y; Department of Neurology.
Wang S; Department of Neurology.
Wang C; Department of Neurology.
Lu Y; Department of Neurology.
Xi J; Department of Neurology.
Lu Q; Department of Neurology.
Chen Y; Department of Neurology.

Medicine (Baltimore) ; 97(17): e0347, 2018 Apr.

Article en En | MEDLINE | ID: mdl-29702980

Asunto(s)

Síndromes Miasténicos Congénitos/genética; Receptores Nicotínicos/genética; Pueblo Asiatico; Preescolar; China; Humanos; Masculino; Mutación

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores Nicotínicos / Síndromes Miasténicos Congénitos Tipo de estudio: Prognostic_studies Límite: Child, preschool / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Medicine (Baltimore) Año: 2018 Tipo del documento: Article

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