Autosomal dominant cerebellar ataxias
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
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1. Autosomal Dominant Spinocerebellar Ataxias and Episodic Ataxias;Handbook of the Cerebellum and Cerebellar Disorders;2021-12-05
2. Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia;Proceedings of the National Academy of Sciences;2020-03-04
3. Visual Loss;Liu, Volpe, and Galetta's Neuro-Ophthalmology;2019
4. A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies;Brain;2017-04-21
5. A homozygous mutation ofVWA3Bcauses cerebellar ataxia with intellectual disability;Journal of Neurology, Neurosurgery & Psychiatry;2015-07-08
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