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.

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https://hal-univ-tln.archives-ouvertes.fr/hal-01874181
Contributor : Mathieu Gruet <>
Submitted on : Friday, September 14, 2018 - 10:11:49 AM
Last modification on : Friday, July 26, 2019 - 12:34:03 PM

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  • HAL Id : hal-01874181, version 1

Citation

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.. Journal of Physiology, Wiley, 2017. ⟨hal-01874181⟩

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