(Q81693686)
Statements
Homozygosity for L997F in a child with normal clinical and chloride secretory phenotype provides evidence that this cystic fibrosis transmembrane conductance regulator mutation does not cause cystic fibrosis (English)
Derichs N
Schuster A
Grund I
Ernsting A
Stolpe C
Körtge-Jung S
Gallati S
Kozlowski P