ArticleAmerican journal of human genetics2008
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.
Alexander G Bassuk et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
119 papers cite itlatest 60 shown
this papercites it