Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Reference40 articles.
1. Marcoglis RL. Dominant spinocerebellar ataxias: a molecular approach to classification, diagnosis, pathogenesis and the future. Expert Rev Mol Diagn. 2003;3(6):715–32.
2. Durr A. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond. Lancet Neurol. 2010;9:885–94.
3. Deppont C, Donatello S, Rai M, Wang FC, Manto M, Simonmis N, et al. MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43). Neurol Genet. 2016;2:1–6.
4. Didonna A, Opal P. Advances in sequencing technologies for understanding hereditary ataxias. JAMA Neurol. 2016;17:1–6.
5. Pulst SM, Nechiporuk A, Nechiporuk T, Gispert S, Chen XN, Lopes-Cendes I, et al. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nat Genet. 1996;14(3):269–76.
https://doi.org/10.1038/ng1196-269
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