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Overcoming the Divide Between Ataxias and Spastic Paraplegias: Shared Phenotypes, Genes, and Pathways

Autosomal-dominant spinocerebellar ataxias, autosomal-recessive spinocerebellar ataxias, and hereditary spastic paraplegias have traditionally been designated in separate clinicogenetic disease classifications. This classification system still largely frames clinical thinking and genetic workup in c...

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Détails bibliographiques
Publié dans:Mov Disord
Auteurs principaux: Synofzik, Matthis, Schüle, Rebecca
Format: Artigo
Langue:Inglês
Publié: 2017
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6287914/
https://ncbi.nlm.nih.gov/pubmed/28195350
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.26944
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