A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides.

Highsmith, W E

A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides. [electronic resource] - Clinical genetics Jul 2005 - 88-90 p. digital

Publication Type: Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

0009-9163

10.1111/j.1399-0004.2005.00459.x doi


Aged
Chlorides
Cystic Fibrosis--etiology
Cystic Fibrosis Transmembrane Conductance Regulator--genetics
Family
Female
Humans
Lung Diseases--etiology
Male
Middle Aged
Mutation
Reference Values
Sweat