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Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan.

beta-Thalassemia is a hereditary disease caused by any of 90 different point mutations in the beta-globin gene. Specific populations generally carry a small number of mutations, the most common of which are those that are widely distributed regionally. The present study constitutes an extensive mole...

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Sparad:
I publikationen:Proc Natl Acad Sci U S A
Huvudupphov: Rund, D, Cohen, T, Filon, D, Dowling, C E, Warren, T C, Barak, I, Rachmilewitz, E, Kazazian, H H, Oppenheim, A
Materialtyp: Artigo
Språk:Inglês
Utgiven: National Academy of Sciences 1991
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC50800/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1986379/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.88.1.310
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