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Heterozygosity of the Alpha 1‐Antitrypsin PiZ Allele and Risk of Liver Disease

Heterozygosity of the Alpha 1‐Antitrypsin PiZ Allele and Risk of Liver Disease

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_12ecadbc09b84d74be1f2c5fa3d2dfa5

Heterozygosity of the Alpha 1‐Antitrypsin PiZ Allele and Risk of Liver Disease

About this item

Full title

Heterozygosity of the Alpha 1‐Antitrypsin PiZ Allele and Risk of Liver Disease

Publisher

United States: John Wiley & Sons, Inc

Journal title

Hepatology Communications, 2021-08, Vol.5 (8), p.1348-1361

Language

English

Formats

Publication information

Publisher

United States: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

The serpin family A member 1 (SERPINA1) Z allele is present in approximately one in 25 individuals of European ancestry. Z allele homozygosity (Pi*ZZ) is the most common cause of alpha 1‐antitrypsin deficiency and is a proven risk factor for cirrhosis. We examined whether heterozygous Z allele (Pi*Z) carriers in United Kingdom (UK) Biobank, a popul...

Alternative Titles

Full title

Heterozygosity of the Alpha 1‐Antitrypsin PiZ Allele and Risk of Liver Disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_12ecadbc09b84d74be1f2c5fa3d2dfa5

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_12ecadbc09b84d74be1f2c5fa3d2dfa5

Other Identifiers

ISSN

2471-254X

E-ISSN

2471-254X

DOI

10.1002/hep4.1718

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