about
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations.Niemann-Pick disease: a frequent missense mutation in the acid sphingomyelinase gene of Ashkenazi Jewish type A and B patientsThe presence of two different infantile Tay-Sachs disease mutations in a Cajun populationElevated frequency of Tay-Sachs disease among Ashkenazic Jews unlikely by genetic drift aloneRecent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: positive selection is not always necessary to account for disease incidence among Ashkenazi Jews.Selection in favor of lysosomal storage disorders?Heterozygote advantage in Tay-Sachs carriers?Marital mores as a mechanism for the maintenance of ethnic variations of lethal gene frequenciesBloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim.The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin.Analytic review: some current problems of human population genetics.Large deviations in the distribution of rare genes.Ethnic variation in genetic disease: possible roles of hitchhiking and epistasis.The first arrival time and mean age of a deleterious mutant gene in a finite population.Founder effect in Tay-Sachs disease.
P2860
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P2860
description
1972 nî lūn-bûn
@nan
1972年の論文
@ja
1972年論文
@yue
1972年論文
@zh-hant
1972年論文
@zh-hk
1972年論文
@zh-mo
1972年論文
@zh-tw
1972年论文
@wuu
1972年论文
@zh
1972年论文
@zh-cn
name
Founder effect in Tay-Sachs disease unlikely
@ast
Founder effect in Tay-Sachs disease unlikely
@en
type
label
Founder effect in Tay-Sachs disease unlikely
@ast
Founder effect in Tay-Sachs disease unlikely
@en
prefLabel
Founder effect in Tay-Sachs disease unlikely
@ast
Founder effect in Tay-Sachs disease unlikely
@en
P2093
P1476
Founder effect in Tay-Sachs disease unlikely
@en
P2093
Aronson SM
Myrianthopoulos NC
P2860
P304
P407
P577
1972-05-01T00:00:00Z