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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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
1991
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| Témata: | |
| On-line přístup: | 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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