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Cystic fibrosis genetic basis

T Defects in protein folding may be the molecular basis for a wide range of human genetic disorders. For example, cystic fibrosis is caused by defects in a membrane-bound protein called cystic /ibrosis transmembrane conductance regulator (CFTR), which acts as a channel for chloride ions. The most common cystic... [Pg.149]

Chu CS, Trapnell BC, Curristin S, Cutting GR, Crystal RG. Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA. Nat Genet 1993 3 151. [Pg.137]

See other pages where Cystic fibrosis genetic basis is mentioned: [Pg.178]    [Pg.72]    [Pg.300]    [Pg.358]    [Pg.454]    [Pg.457]    [Pg.52]    [Pg.128]    [Pg.392]    [Pg.14]    [Pg.554]    [Pg.178]    [Pg.128]    [Pg.311]    [Pg.24]    [Pg.223]    [Pg.382]    [Pg.1402]    [Pg.687]    [Pg.148]    [Pg.195]    [Pg.178]    [Pg.65]    [Pg.1262]    [Pg.87]    [Pg.193]    [Pg.346]   
See also in sourсe #XX -- [ Pg.358 ]



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Cystic fibrosis

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