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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Detalhes bibliográficos

Publicado no:	J Clin Invest
Principais autores:	Lawler, Jack, Liu, Shih-Chun, Palek, Jiri, Prchal, Josef
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Clinical Investigation 1982
Assuntos:	Articles
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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