𝔖 Bobbio Scriptorium
✦   LIBER   ✦

CFTR gene and cystic fibrosis


Book ID
108949838
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
32 KB
Volume
19
Category
Article
ISSN
0815-9319

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πŸ“œ SIMILAR VOLUMES


Incidence and expression of the N1303K m
✍ L. Osborne; G. Santis; M. Schwarz; K. Klinger; T. DΓΆrk; I. McIntosh; M. Schwartz πŸ“‚ Article πŸ“… 1992 πŸ› Springer 🌐 English βš– 590 KB

The N1303K mutation was identified in the second nucleotide binding fold of the cystic fibrosis (CF) gene last year. We have gathered data from laboratories throughout Europe and the United States of America in order to estimate its frequency and to attempt to characterise the clinical manifestation

Heterogeneity in the severity of cystic
✍ Michael Dean; George Santis πŸ“‚ Article πŸ“… 1994 πŸ› Springer 🌐 English βš– 589 KB

Cystic fibrosis is a common, fatal disorder caused by abnormalities in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. CFTR encodes a chloride channel that regulates secretion in many exocrine tissues. The presentation of cystic fibrosis is highly variable as measured by the age