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; Julie Larribaut; Thierry Troosters; Samuel Verges

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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Mathieu Gruet

Function : Author
PersonId : 750670
IdHAL : mathieu-gruet
ORCID : 0000-0002-2658-277X
IdRef : 157618900

Université de Toulon

Laboratoire Motricité Humaine Expertise Sport Santé

Laboratoire Motricité Humaine Expertise Sport Santé/Equipe de recherche de Toulon

Julie Larribaut

Function : Author

Thierry Troosters

Function : Author

Samuel Verges

Function : Author
PersonId : 919185

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Tissues and Organs [q-bio.TO]

MATHIEU GRUET : Connect in order to contact the contributor

https://hal-univ-tln.archives-ouvertes.fr/hal-01874181

Submitted on : Friday, September 14, 2018-10:11:49 AM

Last modification on : Thursday, August 4, 2022-4:59:55 PM

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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⟩

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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