𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Aberrant CFTR-dependent HCO-3 transport in mutations associated with cystic fibrosis

✍ Scribed by Choi, Joo Young; Muallem, Daniella; Kiselyov, Kirill; Lee, Min Goo; Thomas, Philip J.; Muallem, Shmuel


Book ID
109773837
Publisher
Nature Publishing Group
Year
2001
Tongue
English
Weight
321 KB
Volume
410
Category
Article
ISSN
0028-0836

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Population screening if F508del (Ξ”F508),
✍ MarΓ­a RoquΓ©; Clara Pott Godoy; Mariana Castellanos; Eduardo Pusiol; Luis S. Mayo πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 35 KB

Cystic fibrosis (CF) is the most common autosomal recessive disease in the Caucasian population. The disease can be caused by one of the more than 900 different mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene. However, the deletion of the phe508-codon is the most pre