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. - Archive ouverte HAL Access content directly
Journal Articles The Journal of Physiology Year : 2017

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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hal-01874181 , version 1 (14-09-2018)

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  • HAL Id : hal-01874181 , version 1

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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⟩
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