Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chains.
An abnormal spectrin, in which one subunit is truncated, has been detected in a large German family. The inheritance is autosomal dominant. The affected members of the family suffer in widely varying degree from a microcytic hemolytic anemia. The red cell morphology varies correspondingly from smoot...
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| Udgivet i: | J Clin Invest |
|---|---|
| Principais autores: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society for Clinical Investigation
1988
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC329600/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3276733/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI113350 |
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