Follow-up and genetic study of 43 Chinese children with type Ⅰ Alexander disease

Objective: To identify the clinical and genetic characteristics in 43 Chinese children diagnosed with type Ⅰ Alexander disease (AxD). Method: Forty-three type Ⅰ AxD cases identified by glial fibrillary acidic protein (GFAP) gene mutations in Peking University First Hospital from 2005 to 2016 were fo...

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Veröffentlicht in:	Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 55(2017), 7 vom: 02. Juli, Seite 504-508
1. Verfasser:	Ban, T T (VerfasserIn)
Weitere Verfasser:	Wu, Y, Zhang, Z B, Zang, L L, Wang, J M, Jiang, Y W
Format:	Online-Aufsatz
Sprache:	Chinese
Veröffentlicht:	2017
Zugriff auf das übergeordnete Werk:	Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:	Journal Article Alexander disease Follow-up studies Genes Glial fibrillary acidic protein Glial Fibrillary Acidic Protein