A nucleotide change at a splice junction in the human beta-globin gene is associated with beta 0-thalassemia.
beta 0-Thalassemia is a heterogeneous group of disorders associated with absence of beta-globin. In a survey of DNAs from patients with beta 0-thalassemia of diverse ethnic origins, a change at the splice junction at the 5' end of the large intervening sequence (IVS 2) of the human beta-globin gene...
Tallennettuna:
| Julkaisussa: | Proc Natl Acad Sci U S A |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
National Academy of Sciences
1981
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC319760/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6270663/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.78.7.4218 |
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