Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.
The deletions in the zeta-alpha globin gene cluster in two infants with the hemoglobin Bart's hydrops fetalis syndrome (homozygous alpha thalassemia 1) have been mapped by restriction endonuclease analysis using a zeta-specific probe. DNA from a Thai infant lacked the psi alpha 1 gene and both alpha...
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| Published in: | Proc Natl Acad Sci U S A |
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| Main Authors: | , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
National Academy of Sciences
1980
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC349662/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6158051/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.77.6.3586 |
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