HLA phenotypes and gene polymorphisms in juvenile liver disease associated with α1-antitrypsin deficiency-Reference-Cited by-同舟云学术

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HLA phenotypes and gene polymorphisms in juvenile liver disease associated with α1-antitrypsin deficiency

Published:1990-08 Issue:2 Volume:12 Page:218-223
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Doherty Derek G.,Donaldson Peter T.,Whitehouse David B.,Mieli-Vergani Giorgina,Duthie Ann,Hopkinson David A.,Mowat Alex P.

Publisher

Wiley

Subject

Hepatology

Reference40 articles.

1. Molecular basis of alpha-1-antitrypsin deficiency

2. Outcome of liver disease associated with alpha 1 antitrypsin deficiency (PiZ). Implications for genetic counselling and antenatal diagnosis.

3. Variation in alpha-1-antitrypsin phenotypes associated with penicillamine therapy

4. . The Pi polymorphism: genetic, biochemical and clinical aspects of human α1-antitrypsin. In: , eds. Advances in human genetics 11. New York and London: Plenum Press, 1981: 1–62.

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2. Elevated soluble HLA II protein levels in patients with alpha-1 antitrypsin deficiency with or without COPD;Experimental Lung Research;2012-06-11

3. α1-Antitrypsin Deficiency;Molecular Pathology Library;2010-11-02

4. Cholestasis in Neonates and Infants;Gastroenterology and Nutrition: Neonatology Questions and Controversies;2008

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