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

Author: Wei-Dong ZHOU ¹ ; Cheng-Hao LIU ² ; Xiao-Min YIN ³ ; Qing-Yu ZENG ³
Author Information

1. 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.
2. Department of Neurology, Graduate School, North China University of Science and Technology, Tangshan, Hebei 063015, China.
3. Department of Radiology, China Meitan General Hospital, Beijing 100028, China.
Publication Type:Case Reports
MeSH: Adult; Asian Continental Ancestry Group; Female; Filamins; genetics; Humans; Mutation; genetics; Periventricular Nodular Heterotopia; genetics; pathology
From: Chinese Medical Journal 2016;129(18):2262-2263
CountryChina
Language:English