LRRK2 gene mutation⁃associated semantic variant primary progressive aphasia: one case report and literatures review

LRRK2 gene mutation⁃associated semantic variant primary progressive aphasia: one case report and literatures review

Objective To report the clinical phenotype and gene mutation characteristics of a case with leucine⁃rich repeat kinase 2 (LRRK2) gene mutation⁃associated semantic variant primary progressive aphasia. Methods and Results The clinical data of a patient with language comprehension impairment as the fir...

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Bibliographic Details
Main Authors: Shi-peng GUO, Da-ning CHEN, Xiao-yang LEI, An-ni ZHANG, Xu-ling WU, Ya LI, Dian HE
Format: Article
Language:English
Published: Tianjin Huanhu Hospital 2020-06-01
Series:Chinese Journal of Contemporary Neurology and Neurosurgery
Subjects:
aphasia,primaryprogressive
frontotemporaldementia
genes
mutation
Online Access:http://www.cjcnn.org/index.php/cjcnn/article/view/2151

Internet

http://www.cjcnn.org/index.php/cjcnn/article/view/2151

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