Defective spectrin dimer-dimer association with hereditary elliptocytosis.
We examined erythrocytes from 18 patients with hereditary elliptocytosis. Spectrin from eight patients (referred to as type 1) was defective in dimer-dimer association as demonstrated in two ways. First, there was an increased amount of spectrin dimer with a concomitant decrease in tetramer as measu...
Sparad:
| I publikationen: | Proc Natl Acad Sci U S A |
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| Huvudupphov: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Utgiven: |
National Academy of Sciences
1982
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC346125/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6952254/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.79.6.2072 |
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