Association between heterozygous β1-antitrypsin deficiency and genetic hemochromatosis-Reference-Cited by-同舟云学术

Association between heterozygous β1-antitrypsin deficiency and genetic hemochromatosis

Published:1992-07 Issue:1 Volume:16 Page:145-148
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Rabinovitz Mordechai,Gavaler Judith S.,Kelly Robert H.,Van Thiel David H.

Publisher

Wiley

Subject

Hepatology

Reference17 articles.

1. Idiopathic hemochromatosis: A study of biochemical expression in 247 heterozygous members of 63 families: Evidence for a single major HLA-linked gene

2. Heredity of idiopathic haemochromatosis: A study of 106 families

3. The cellular basis for liver injury in α1-antitrypsin deficiency

4. Idiopathic Hemochromotosis and Alpha-1-Antitrypsin Deficiency: Coexistence in a Family with Progressive Liver Disease in the Proband

5. . Alpha-1-antitrypsin deficiency and adult liver disease. In: ed. Protides of the biological fluids. Proceedings of the twenty-third colloquium Brugge, 1975. New York: Pergamon Press, 1975: 383–385.

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