A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin.

At least 35 allelic variants of human serum albumin have been sequenced at the protein level. All except two COOH-terminal variants, Catania and Venezia, are readily explainable as single-point substitutions. The two chain-termination variants are clustered in certain locations in Italy and are foun...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Watkins, S, Madison, J, Davis, E, Sakamoto, Y, Galliano, M, Minchiotti, L, Putnam, F W
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1991
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC52001/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2068071/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.88.14.5959
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