| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4146104 | Archives de Pédiatrie | 2013 | 4 Pages |
Abstract
APK is very frequent in patients with CF. It is most probably a consequence of the dysfunction of the CFTR protein. It should be systematically sought in all patients with CF. Its discovery in another context should suggest the diagnosis of CF or a carriage to the heterozygous state of a mutation involved in the disease.
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Authors
B. Weil, E. Chaillou, F. Troussier, C. Pelatan, M. Chiffoleau, E. Darviot, M.-C. Chevalier, L. Martin, J.-L. Giniès,