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Article

Homozygous bisalbuminemia or homozygous mutant albumin?

Clinical biochemistry - 1 Jan 2012

Kulkarni Ketan, Rowe Pamela, Christensen Cathie Lou, Higgins Trefor

Abstract excerpt

INTRODUCTION: Bisalbuminemia is a genetic condition in which an albumin variant is found in serum in addition to normal albumin. METHODS AND MATERIALS: Serum protein electrophoresis using the Sebia HYDRASYS electrophoresis system was performed on an 84 year old male. RESULTS: Serum protein electrophoresis showed a single albumin band migrating faster than normal albumin. CONCLUSION: The presence of a homozygous...

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Identifiers

PMID: 22040810
DOI: 10.1016/j.clinbiochem.2011.10.005

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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