Molecular basis for dominantly inherited inclusion body beta-thalassemia.
Analysis of the molecular basis of dominantly inherited beta-thalassemia in four families has revealed different mutations involving exon 3 of the beta-globin gene. It is suggested that the phenotypic difference between this condition and the more common recessive forms of beta-thalassemia lies main...
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| 出版年: | Proc Natl Acad Sci U S A |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
1990
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC54016/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1971109/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.10.3924 |
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