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Article

Congenital analbuminaemia diagnosed in adulthood in an Australian family.

Pathology - 1 Aug 2015

Berglund L J, van der Poorten D K, Caridi G, Campagnoli M, Minchiotti L

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 26132898
DOI: 10.1097/PAT.0000000000000288

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Congenital analbuminaemia diagnosed in adulthood in an Australian family.PMID 26132898Read ↗

Pregnancy in a patient with congenital analbuminaemia.Semantic proximity Read ↗

[Congenital analbuminemia].Semantic proximity Read ↗

A novel splicing mutation in the ALB gene causing analbuminaemia in a Portuguese woman.Semantic proximity Read ↗

Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene.Semantic proximity Read ↗

Congenital analbuminaemia: molecular defects and biochemical and clinical aspects.Semantic proximity Read ↗

A novel insertion (c.1098dupT) in the albumin gene causes analbuminemia in a consanguineous family.Semantic proximity Read ↗

A novel nonsense variation in the albumin gene (c.1309 A>T) causing analbuminaemia.Semantic proximity Read ↗

Congenital analbuminemia attributable to compound heterozygosity for novel mutations in the albumin gene.Semantic proximity Read ↗

A novel splicing mutation causes an undescribed type of analbuminemia.Semantic proximity Read ↗

Congenital Analbuminemia in Unrelated Algerian and Turkish Families is Caused by the Same Molecular Defect in the Albumin Gene.Semantic proximity Read ↗

Analbuminemia produced by a novel splicing mutation.Semantic proximity Read ↗

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

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