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American Journal of Human Genetics|November 4, 2008
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndromeAlexander G Bassuk, Robyn H Wallace, Aimee Buhr, et al.American Journal of Human Genetics|February 1, 2011
Mutations in prickle orthologs cause seizures in flies, mice, and humansHirotaka Tao, J Robert Manak, Levi Sowers, et al.Pageof 12