The French Canadian Tay-Sachs disease deletion mutation: identification of probable founders
- 1 April 1992
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 89 (1) , 83-87
- https://doi.org/10.1007/bf00207048
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Founder Effect in Familial Hyperchylomicronemia among French Canadians of QuebecHuman Heredity, 1991
- Allele‐specific amplification of genomic DNA for detection of deletion mutations: Identification of a French‐Canadian tay‐sachs mutationJournal of Inherited Metabolic Disease, 1990
- MORE THAN ONE MUTANT ALLELE CAUSES INFANTILE TAY-SACHS DISEASE IN FRENCH-CANADIANS1990
- Genetic epidemiology of hereditary tyrosinemia in Quebec and in Saguenay-Lac-St-Jean.1990
- A deletion involving Alu sequences in the beta-hexosaminidase alpha-chain gene of French Canadians with Tay-Sachs disease.Journal of Biological Chemistry, 1987
- Different Mutations in Ashkenazi Jewish and Non-Jewish French Canadians with Tay-Sachs DiseaseScience, 1986
- Genetic variants of Tay-Sachs disease: Tay-Sachs disease and Sandhoff's disease in French Canadians, juvenile Tay-Sachs disease in Lebanese Canadians, and a Tay-Sachs screening program in the French-Canadian population.1977
- Tay-Sachs disease in Quebec: evidence for a geographic aggregate in the French-Canadian population and identification of a new retardation syndrome with possible linkage to the Tay-Sachs gene.1973
- Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase ComponentScience, 1969