Caricamento...

Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding.

Hereditary spherocytosis (HS) is an inherited disorder of erythrocyte shape associated with spectrin deficiency and hemolytic anemia. In a subset of patients with the autosomal dominant form of HS, spectrin displays a reduced capacity to bind protein 4.1 and, therefore, actin; both functions that ar...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Becker, P S, Morrow, J S, Lux, S E
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1987
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC442269/
https://ncbi.nlm.nih.gov/pubmed/3611357
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !