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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 12, 2024. (Total: 231400Documents)
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Query Trace: Ataxia and LMNB1[original query]
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia.
Movement disorders : official journal of the Movement Disorder Society 2012 Mar 27 (3): 442-6.
Fogel Brent L, Lee Ji Yong, Lane Jessica, Wahnich Amanda, Chan Sandy, Huang Alden, Osborn Greg E, Klein Eric, Mamah Catherine, Perlman Susan, Geschwind Daniel H, Coppola Giovan
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