Associated Papers
ANO10 Function in Health and Disease.
Chrysanthou A et al.
Cerebellum (london, England), 2023
Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia.
Keogh MJ et al.
Journal of Neurology, 2015
Respiratory chain deficiency in nonmitochondrial disease.
Pyle A et al.
Neurology. Genetics, 2015
ANO10 mutations cause ataxia and coenzyme Q₁₀ deficiency.
Balreira A et al.
Journal of Neurology, 2014
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