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Article

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

Proceedings of the National Academy of Sciences of the United States of America - 15 Jul 1991

Watkins S, Madison J, Davis E, Sakamoto Y, Galliano M, Minchiotti L, Putnam F W

Abstract excerpt

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 found in numerous unrelated individuals. In order to correlate the protein change in these variants with the...

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Identifiers

PMID: 2068071
DOI: 10.1073/pnas.88.14.5959
PMCID: PMC52001

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Source receipt: pubmed, retrieved 7 Sept 2026.

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