Autosomal recessive cerebellar hypoplasia in the Hutterite population
Hannah C. Glass(University of California, San Francisco), D. Ross McLeod(Alberta Children's Hospital), Elaine Wirrell(WinnMed), Karen Barlow(The University of Queensland), Takuya Fujiwara(Montreal General Hospital), Kym M. Boycott(Children's Hospital of Eastern Ontario), James N. Scott, Kenneth Morgan(University of London), Coleen Adams(Victoria General Hospital), Albert E. Chudley(University of Manitoba)
Cited by 41
Related Papers
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
|Nature Genetics|1999|1.7k
Mutations in the Gene for Cardiac Myosin-Binding Protein C and Late-Onset Familial Hypertrophic Cardiomyopathy
|New England Journal of Medicine|1998|759
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes
|Nature Genetics|2012|752