Identification of a novel mutation in the CACNA1C gene in a Chinese family with autosomal dominant cerebellar ataxia

Background Hereditary ataxia is a group of neurodegenerative diseases with progressive cerebellar ataxia of the gait and limbs as the main symptoms. The genetic patterns of the disease are diverse but it is mainly divided into autosomal dominant cerebellar ataxia (ADCA) and autosomal recessive cereb...

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Bibliographic Details
Published in:BMC neurology Vol. 19; no. 1; pp. 157 - 6
Main Authors: Chen, Jiajun, Sun, Yajuan, Liu, Xiaoyang, Li, Jia
Format: Journal Article
Language:English
Published: London BioMed Central 10.07.2019
BioMed Central Ltd
BMC
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ISSN:1471-2377, 1471-2377
Online Access:Get full text
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