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 (Q81693686)
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scientific article published on 01 June 2005
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
scientific article published on 01 June 2005 |
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