Hemoglobin Wayne: a frameshift mutation detected in human hemoglobin alpha chains.
Hemoglobin Wayne is an alpha chain variant which manifests itself as two minor hemoglobin (Hb) components that migrate more rapidly than Hb A on electrophoresis at pH 8.6. It has been found in a child with Fanconi's anemia and in three generations of the child's family. Each of the minor components...
Uloženo v:
| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
1976
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC336023/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1062801/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.73.3.882 |
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