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Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.

Protein 4.1 is an approximately 80-kD structural protein in the membrane skeleton which underlies and supports the erythrocyte plasma membrane. The preceding companion paper presents a biochemical study of two abnormal protein 4.1 species from individuals with the red blood cell disorder, hereditary...

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Detalhes bibliográficos
Publicado no:J Clin Invest
Principais autores: Conboy, J, Marchesi, S, Kim, R, Agre, P, Kan, Y W, Mohandas, N
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 1990
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC296755/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2384598/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114739
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