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Article

[Study of the frequency of different phenotypes of alpha-1-antitrypsin in a population of Barcelona].

Medicina clinica - 6 Jul 1996

Vidal R, Miravitlles M, Jardí R, Torrella M, Rodríguez-Frías F, Moral P, Vaqué J

Abstract excerpt

BACKGROUND: Severe alpha-1-antitrypsin (AAT) deficiency is caused by homozygous inheritance of gene Z, and is associated with a high risk of developing pulmonary emphysema. Determination of frequencies of different genes associated with the deficiency (especially S and Z) gives a clue to estimate...

Topics

Adolescent
Adult
Alleles
Female
France
Gene Frequency
Humans
Italy
Male
Middle Aged
Phenotype
Portugal
Spain

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

United States

alpha 1-Antitrypsin

alpha 1-Antitrypsin Deficiency

Source

Identifiers

PMID: 8755448

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8755448-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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[Study of the frequency of different phenotypes of alpha-1-antitrypsin in a population of Barcelona].PMID 8755448Read ↗

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[Allelic frequency of the gene of alpha-1-antitrypsin in the general population in a county in Asturias].Semantic proximity Read ↗

Frequency of alleles and genotypes associated with alpha-1 antitrypsin deficiency in clinical and general populations: Revelations about underdiagnosis.Semantic proximity Read ↗

[Prevalence of the alpha-1 antitrypsin phenotype in Hungary].Semantic proximity Read ↗

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Alpha-1 antitrypsin deficiency in Italy: regional differences of the PIS and PIZ deficiency alleles.Semantic proximity Read ↗

Alpha1-antitrypsin Pi phenotypes S and Z in Spain: an analysis of the published surveys.Semantic proximity Read ↗

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