Literature DB >> 4784938

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.

E Andermann, F Andermann, G Patry, R Lafontaine, G Geoffroy, C R Scriver, L Wolfe.   

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Year:  1973        PMID： 4784938

Source DB:  PubMed          Journal:  Trans Am Neurol Assoc        ISSN： 0065-9479


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  3 in total

1.  The French Canadian Tay-Sachs disease deletion mutation: identification of probable founders.

Authors:  M De Braekeleer; P Hechtman; E Andermann; F Kaplan
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

2.  Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease.

Authors:  M Cohen-Tannoudji; P Marchand; S Akli; S A Sheardown; J P Puech; C Kress; P Gressens; M C Nassogne; T Beccari; A L Muggleton-Harris
Journal:  Mamm Genome       Date:  1995-12       Impact factor: 2.957

3.  Allele-specific amplification of genomic DNA for detection of deletion mutations: identification of a French-Canadian Tay-Sachs mutation.

Authors:  F Kaplan; B Boulay; J Bayleran; P Hechtman
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982
  3 in total

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