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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| Published in: | BMC neurology Vol. 19; no. 1; pp. 157 - 6 |
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| Main Authors: | , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
London
BioMed Central
10.07.2019
BioMed Central Ltd BMC |
| Subjects: | |
| ISSN: | 1471-2377, 1471-2377 |
| Online Access: | Get full text |
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