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Molecular Defect of Spectrin in Hereditary Pyropoikilocytosis
In hereditary pyropoikilocytosis (HPP) the erythrocyte membrane skeleton exhibits mechanical instability that can be correlated to defective self-association of spectrin heterodimers. To detect structural changes in the functional domains of HPP spectrin we have examined the peptide pattern produced...
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| Publicado no: | J Clin Invest |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
1982
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC370314/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7130392/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI110689 |
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