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Heterozygous Mutations in the ADCK3 Gene in Siblings with Cerebellar Atrophy and Extreme Phenotypic Variability

We describe a highly variable clinical presentation of cerebellar ataxia in two sisters. The younger sister demonstrates early onset rapidly progressive cerebellar ataxia accompanied by motor and nonmotor cerebellar features, as well as cognitive decline and psychiatric problems. Mitochondrial respi...

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Detalhes bibliográficos
Main Authors: Blumkin, Lubov, Leshinsky-Silver, Esther, Zerem, Ayelet, Yosovich, Keren, Lerman-Sagie, Tally, Lev, Dorit
Formato: Artigo
Idioma:Inglês
Publicado em: Springer International Publishing 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3897800/
https://ncbi.nlm.nih.gov/pubmed/24048965
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2013_251
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