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Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.
The interaction of spectrin with spectrin-depleted inside-out membrane vesicles was studied in a kindred with an atypical variant of hereditary elliptocytosis inherited in a recessive manner. The probands are characterized by prominent elliptocytosis, decreased erythrocyte thermal stability, an alte...
Tallennettuna:
| Julkaisussa: | J Clin Invest |
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| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Society for Clinical Investigation
1984
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC425229/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6236232/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI111491 |
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