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B R Akerman

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Molecular Genetics and Metabolism|September 10, 1999
Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohortB R Akerman, H Lemass, L M Chow, et al.
Human Molecular Genetics|May 23, 1998
Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxicationE P Treacy, B R Akerman, L M Chow, et al.
Human Mutation|January 1, 1992
A mutation common in non-Jewish Tay-Sachs disease: frequency and RNA studiesB R Akerman, J Zielenski, B L Triggs-Raine, et al.
American Journal of Human Genetics|October 1, 1992
A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screeningB L Triggs-Raine, E H Mules, M M Kaback, et al.
Human Molecular Genetics|January 1, 1996
Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseasesD Phaneuf, N Wakamatsu, J Q Huang, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Molecular Genetics and Metabolism|September 10, 1999
Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohortB R Akerman, H Lemass, L M Chow, et al.
Human Molecular Genetics|May 23, 1998
Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxicationE P Treacy, B R Akerman, L M Chow, et al.
Human Mutation|January 1, 1992
A mutation common in non-Jewish Tay-Sachs disease: frequency and RNA studiesB R Akerman, J Zielenski, B L Triggs-Raine, et al.
American Journal of Human Genetics|October 1, 1992
A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screeningB L Triggs-Raine, E H Mules, M M Kaback, et al.
Human Molecular Genetics|January 1, 1996
Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseasesD Phaneuf, N Wakamatsu, J Q Huang, et al.
Pageof 2