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Article

Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene.

Clinical biochemistry - 1 Sept 2005

Campagnoli Monica, Sala Alberto, Labò Sara, Rossi Antonio, Neuhaus Thomas J, Braegger Christian P, Minchiotti Lorenzo, Galliano Monica

Abstract excerpt

OBJECTIVE: To define the molecular defect that causes analbuminemia in an apparently healthy boy, son of non-consanguineous Swiss parents. DESIGN AND METHODS: Total DNA, extracted from peripheral blood samples from the proband and from both parents, was PCR-amplified using oligonucleotide primers designed to amplify the 14 exons of the human albumin gene and the flanking intron regions. The products were screened...

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Identifiers

PMID: 15996651
DOI: 10.1016/j.clinbiochem.2005.05.013

Genes

CGA

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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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