Human Genome Epidemiology Literature Finder
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Query Trace: Atrophy and KCNC3[original query] |
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Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia. Clinical genetics 2016 Apr . Barresi S, Niceta M, Alfieri P, Brankovich V, Piccini G, Bruselles A, Barone M R, Cusmai R, Tartaglia M, Bertini E, Zanni |
- Page last reviewed:Feb 1, 2024
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