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No association between genetic hemochromatosis and alpha1-antitrypsin deficienc

✍ Scribed by S Fargion; F Bissoli; AL Fracanzani; E Suigo; C Sergi; E Taioli; R Ceriani; V Dimasi; A Piperno; M Sampietro; G Fiorelli


Book ID
118686459
Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
167 KB
Volume
24
Category
Article
ISSN
0270-9139

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πŸ“œ SIMILAR VOLUMES


No association between genetic hemochrom
✍ S Fargion; F Bissoli; A L Fracanzani; E Suigo; C Sergi; E Taioli; R Ceriani; V D πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 164 KB

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

Association between heterozygous Ξ²1-anti
✍ Mordechai Rabinovitz; Judith S. Gavaler; Robert H. Kelly; David H. Van Thiel πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 441 KB

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

No association between alpha-1-antichymo
✍ Kim, K.W.; Jhoo, J.H.; Lee, K.U.; Lee, D.Y.; Lee, J.H.; Youn, J.Y.; Lee, B.J.; H πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 19 KB πŸ‘ 3 views

To examine the possible involvement of the alpha-1-antichymotrypsin gene (ACT) polymorphism in the manifestation of Alzheimer's disease (AD), we analyzed genotypes of the ACT and apolipoprotein E gene (APOE) among 110 Korean patients with probable AD and 209 nondemented controls. No significant diff