CFTR and Cystic Fibrosis

Please use this identifier to cite or link to this item: 192.168.6.56/handle/123456789/74859

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DC Field	Value	Language
dc.contributor.author	M. Farinha, Carlos	-
dc.date.accessioned	2019-07-02T08:25:19Z	-
dc.date.available	2019-07-02T08:25:19Z	-
dc.date.issued	2018	-
dc.identifier.isbn	978-3-319-65494-2	en
dc.identifier.uri	http://10.6.20.12:80/handle/123456789/74859	-
dc.description	Cystic fibrosis (CF) is a monogenic autosomal recessive disorder that affects Caucasian individuals. Clinically it is characterized by chronic pulmonary dysfunction, pancreatic insufficiency, increased saline concentration in sweat, and male infertility. The gene responsible for the disease was cloned in 1989 and encodes an ABC transporter, the 1480-amino acid protein named Cystic Fibrosis Transmembrane Conductance Regulator (CFTR), that functions as a chloride (Cl-) channel in the apical membrane of epithelial cells.	en
dc.language.iso	en	en_US
dc.publisher	Springer imprint is published by Springer Nature	en_US
dc.subject	Cystic Fibrosis	en_US
dc.title	CFTR and Cystic Fibrosis	en_US
dc.type	Book	en_US
Appears in Collections:	Chemistry

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