A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome

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A Simple Composite Phenotype Scoring System for Evaluating Mouse Models of Cerebellar Ataxia
07:33

A Simple Composite Phenotype Scoring System for Evaluating Mouse Models of Cerebellar Ataxia

Published on: May 21, 2010

Alexander G Bassuk1, Robyn H Wallace, Aimee Buhr

  • 1Department of Pediatrics, University of Iowa, Iowa City, IA 52242, USA.

American Journal of Human Genetics
|November 4, 2008
PubMed

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