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@UNKBiol106LF A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome #106Week12LFS20 https://t.co/E5nPpB3A3O
A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome
Overview of attention for article published in American Journal of Human Genetics, October 2008
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