Molecular genetics of chronic liver diseases

Author:

Brind A.M.,Bassendine M.F.

Publisher

Elsevier BV

Subject

Gastroenterology,Gastroenterology

Reference115 articles.

1. Prenatal diagnosis of α1-antitrypsin deficiency using polymerase chain reaction;Abbott;Lancet,1988

2. Isolation of a human ferritin receptor;Adams;Hepatology,1988

3. Genetic variation in alcohol metabolizing enzymes-implications in alcohol use and abuse;Agarwal;Progress in Clinical and Biological Research,1987

4. Transferrin receptors in hemochromatosis;Anderson;Hepatology,1987

5. Iron overload complicating sideroblastic anemia: is the gene for hemochromatosis responsible?;Barron;Gastroenterology,1989

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1. Gastrointestinal System;A Practical Guide to Human Cancer Genetics;2013-08-14

2. Erythrocytic Pyruvate Kinase Mutations Causing Hemolytic Anemia, Osteosclerosis, and Secondary Hemochromatosis in Dogs;Journal of Veterinary Internal Medicine;2012-07

3. The prevalence of hereditary haemochromatosis in a diabetic population;QJM;1997-04-01

4. Hemochromatosis in Salers Cattle;Journal of Veterinary Internal Medicine;1994-03

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