๐”– Bobbio Scriptorium
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What is the role of the non-coding regions of the CFTR gene in cystic fibrosis?

โœ Scribed by Castaldo, Giuseppe; Tomaiuolo, Rossella


Book ID
120833646
Publisher
Expert Reviews
Year
2013
Tongue
English
Weight
842 KB
Volume
7
Category
Article
ISSN
1747-6348

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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