Autosomal dominant cerebellar ataxia with dementla: Evidence for a fourth disease locus
The autosomal dominant cerebellar ataxias have proved particularly difficult to classify due to the lack of phenotypic concordance both within and between families. Genetic heterogenelty has been established, and disease loci for spinal cerebellar ataxia have been assigned to chromosomes 6 (SCA1), 1...
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Main Authors: | , , , , , , , , , , , , |
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Format: | Article |
Published: |
2018
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Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/9544 |
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Institution: | Mahidol University |