𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Origin and implication of the hereditary pancreatitis-associated N21I mutation in the cationic trypsinogen gene

✍ Scribed by J.-M. Chen; C. Ferec

Book ID
106137210
Publisher
Springer
Year
2000
Tongue
English
Weight
45 KB
Volume
106
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Mutations of the cationic trypsinogen in
Mutations of the cationic trypsinogen in hereditary pancreatitis
✍ Niels Teich; Joachim MΓΆssner; Volker Keim πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 168 KB

Hereditary pancreatitis (OMIM 167800) is thought to be associated with a mutation of the exon 3 of cationic trypsinogen (Nature Genet (1996): 14:141-145). This paper reports sequence data of two independent families suffering from this disease. PCR amplificates from leukocyte or buccal swab DNA show

Mutation analysis of the HFE gene associ
Mutation analysis of the HFE gene associated with hereditary hemochromatosis in African Americans
✍ Monaghan, Kristin G.; Rybicki, Benjamin A.; Shurafa, Muhammad; Feldman, Gerald L πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 155 KB πŸ‘ 2 views

Homozygosity for the mutation Cys282Tyr in the HFE gene has recently been identified as a cause of hereditary hemochromatosis, a disorder resulting in the inappropriate absorption of iron. Approximately 10% of Caucasians are heterozygous for this mutation; however, the gene frequency in African Amer