Article
Late-onset autosomal recessive cerebellar ataxia and neuropathy with a novel splicing mutation in the ATM gene.
Journal of integrative neuroscience - 30 Mar 2020
Shimazaki Haruo, Kobayashi Junya, Sugaya Ryo, Nakano Imaharu, Fujimoto Shigeru
Abstract excerpt
Autosomal recessive cerebellar ataxias comprise many types of diseases. The most frequent autosomal recessive cerebellar ataxias are Friedreich ataxia, but other types are relatively rare. We encountered a consanguineous family with two cases of late-onset cerebellar ataxia with neuropathy. We performed whole-exome sequencing in one patient and confirmed by Sanger sequencing in other family members. Neurological...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
