Molecular analysis of juvenile Huntington disease: the major influence on (CAG)<sub>n</sub> repeat length is the sex of the affected parent
H. Telenius(University of British Columbia), Michael R. Hayden(Family Research Institute), Amanda E. Starr(University of British Columbia), Jacquie Greenberg(University of Cape Town), F. Squltierl(University of British Columbia), Hannie Kremer(Radboud University Nijmegen), G Lucotte, J. Thellmann(University of British Columbia), Susan E. Andrew(Medical Genetics Center), E. Almqvist(Karolinska Institutet), Y. Paul Goldberg(Agile Therapeutics (United States)), Maria Anvret(Karolinska University Hospital), Cheryl R. Greenberg(University of Manitoba)
Cited by 210
Related Papers
Huntington disease
|Nature Reviews Disease Primers|2015|1.6k
Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis
|Nature Genetics|2003|976
Localization of the gene for Cowden disease to chromosome 10q22–23
|Nature Genetics|1996|670