A Novel Mutation of Filamin A Gene in a Chinese Family with Periventricular Nodular Heterotopia.

Zhou, Wei-Dong; Liu, Cheng-Hao; Yin, Xiao-Min; Zeng, Qing-Yu

Zhou, Wei-Dong; Liu, Cheng-Hao; Yin, Xiao-Min; Zeng, Qing-Yu.

Afiliación

Zhou WD; Department of Neurology, China Meitan General Hospital, Beijing 100028; Department of Neurology, Graduate School, North China University of Science and Technology, Tangshan, Hebei 063015, China.
Liu CH; Department of Neurology, Graduate School, North China University of Science and Technology, Tangshan, Hebei 063015, China.
Yin XM; Department of Radiology, China Meitan General Hospital, Beijing 100028, China.
Zeng QY; Department of Radiology, China Meitan General Hospital, Beijing 100028, China.

Chin Med J (Engl) ; 129(18): 2262-3, 2016 09 20.

Article en En | MEDLINE | ID: mdl-27625105

Asunto(s)

Heterotopia Nodular Periventricular/genética; Adulto; Pueblo Asiatico; Femenino; Filaminas/genética; Humanos; Mutación/genética; Heterotopia Nodular Periventricular/patología

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Heterotopia Nodular Periventricular Límite: Adult / Female / Humans Idioma: En Revista: Chin Med J (Engl) Año: 2016 Tipo del documento: Article País de afiliación: China

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