Larger studies controlling for CFTR class mutations are necessary to infer on the potential presence of an intrinsic skeletal muscle function deficit in patients with cystic fibrosis.

Mathieu Gruet (1, 2, 3) , Julie Larribaut , Thierry Troosters , Samuel Verges

1 UTLN - Université de Toulon
2 LAMHESS - Laboratoire Motricité Humaine Expertise Sport Santé
3 LAMHESS-Toulon - Laboratoire Motricité Humaine Expertise Sport Santé/Equipe de recherche de Toulon

Domaines: Physiologie [q-bio.TO]

Mathieu Gruet, Julie Larribaut, Thierry Troosters, Samuel Verges. Larger studies controlling for CFTR class mutations are necessary to infer on the potential presence of an intrinsic skeletal muscle function deficit in patients with cystic fibrosis.. The Journal of Physiology, 2017. ⟨hal-01874181⟩