Essential hypertension genetics, HLA associations, and heterozygous hemochromatosis
โ Scribed by Jerome L. Sullivan
- Book ID
- 115684546
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 141 KB
- Volume
- 95
- Category
- Article
- ISSN
- 1555-7162
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๐ SIMILAR VOLUMES
Primary hemochromatosis is a genetically determined autosomal recessive disorder characterized by the excessive accumulation of body iron, most of which is deposited in the parenchymal cells of various organs. a,-Antitrypsin deficiency is characterized among others by defective secretion of a,-anti
Mieli-Vergani G. Value of urinary copper excretion after penicillamine challenge in the diagnosis of Wilson's disease. HEPATOLOGY
We previously reported five families with primary, genetic (idiopathic) hemochromatosis in whom HLA typing of subjects indicated that a homozygous-heterozygous mating had almost certainly occurred and in whom inheritance of the disease trait was best explained by an autosomal recessive mode of inher