Lack of Association between Hemochromatosis and α-Antitrypsin Deficiency
✍ Scribed by ERIKSSON, STEN ;LINDMARK, BERTIL ;OLSSON, SIGVARD
- Book ID
- 114694241
- Publisher
- Wiley (Blackwell Publishing)
- Year
- 2009
- Weight
- 247 KB
- Volume
- 219
- Category
- Article
- ISSN
- 0001-6101
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Mieli-Vergani G. Value of urinary copper excretion after penicillamine challenge in the diagnosis of Wilson's disease. HEPATOLOGY
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
synthesized in the liver and is regulated by a gene located Genetic hemochromatosis and a 1 -antitrypsin (AAT) on chromosome 14 for which several alleles have been dedeficiency are frequent in white populations. Conflictscribed. The most common allele, PiM, is associated with an ing data on the asso