Other spinocerebellar ataxias
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Elsevier
Reference58 articles.
1. Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia;Amino;J Hum Genet,2007
2. Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype;Bauer;J Med Genet,2004
3. Autosomal dominant sensory/motor neuropathy with ataxia (SMNA): linkage to chromosome 7q22-q32;Brkanac;Am J Med Genet,2002
4. Spinocerebellar ataxia associated with mutation in the fibroblast growth factor 14 gene (SCA 27): a new phenotype;Brusse;Mov Disord,2006
5. SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2;Cagnoli;Brain,2006
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease;The American Journal of Human Genetics;2024-01
2. Cognitive Changes in the Spinocerebellar Ataxias Due to Expanded Polyglutamine Tracts: A Survey of the Literature;Brain Sciences;2017-07-14
3. Genetic Cerebellar Ataxias;Seminars in Neurology;2014-09-05
4. The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability;Journal of Neurology, Neurosurgery & Psychiatry;2014-08-18
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