Locus assignment of alpha-globin structural mutations by hybrid-selected translation.
The two human alpha-globin genes, alpha 1 and alpha 2 located 3.4 kilobases apart on chromosome 16, encode identical alpha-globin proteins. A mutation in either gene could result in a structural hemoglobinopathy. It has only recently become possible to assign an alpha-chain mutant to one of these tw...
محفوظ في:
| الحاوية / القاعدة: | J Clin Invest |
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| المؤلفون الرئيسيون: | , |
| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
American Society for Clinical Investigation
1985
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| الموضوعات: | |
| الوصول للمادة أونلاين: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC423400/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2981252/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI111698 |
| الوسوم: |
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