Type II Alexander disease with fragile X mental retardation 1 gene mutation.

Xu, Sui-Yi; Liang, Jian-Lin; Li, Hui-Juan; Zhao, Rong-Juan; Li, Chang-Xin

Xu, Sui-Yi; Liang, Jian-Lin; Li, Hui-Juan; Zhao, Rong-Juan; Li, Chang-Xin.

Afiliación

Xu SY; Department of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, Shanxi Province, China.
Liang JL; Department of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, Shanxi Province, China.
Li HJ; Department of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, Shanxi Province, China; Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan Province, China.
Zhao RJ; Department of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, Shanxi Province, China.
Li CX; Department of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, Shanxi Province, China. Electronic address: lichangxin0351@sina.com.

Clin Neurol Neurosurg ; 211: 107023, 2021 12.

Article en En | MEDLINE | ID: mdl-34800814

Asunto(s)

Enfermedad de Alexander/diagnóstico; Enfermedad de Alexander/genética; Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil/genética; Mutación/genética; Humanos; Masculino; Persona de Mediana Edad; Linaje

Palabras clave

Alexander disease; FMR1 gene; GFAP gene; Medulla oblongata atrophy

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Alexander / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Mutación Límite: Humans / Male / Middle aged Idioma: En Revista: Clin Neurol Neurosurg Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos

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