Title : Cystic fibrosis transmembrane conductance regulator modulators for cystic fibrosis: a new dawn?

Pub. Date : 2021 Oct

PMID : 33785533






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 It is a multisystem autosomal recessive disorder caused by variants in the gene for cystic fibrosis transmembrane conductance regulator (CFTR) protein, a cell-surface localised chloride channel that regulates absorption and secretion of salt and water across epithelia. Water CF transmembrane conductance regulator Homo sapiens
2 It is a multisystem autosomal recessive disorder caused by variants in the gene for cystic fibrosis transmembrane conductance regulator (CFTR) protein, a cell-surface localised chloride channel that regulates absorption and secretion of salt and water across epithelia. Water CF transmembrane conductance regulator Homo sapiens