Genetic modifiers of respiratory function in Duchenne muscular dystrophy

OBJECTIVE: Respiratory insufficiency is a major complication of Duchenne muscular dystrophy (DMD). Its progression shows considerable interindividual variability, which has been less thoroughly characterized and understood than in skeletal muscle. We collected pulmonary function testing (PFT) data f...

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Détails bibliographiques
Publié dans:Ann Clin Transl Neurol
Auteurs principaux: Bello, Luca, D’Angelo, Grazia, Villa, Matteo, Fusto, Aurora, Vianello, Sara, Merlo, Beatrice, Sabbatini, Daniele, Barp, Andrea, Gandossini, Sandra, Magri, Francesca, Comi, Giacomo P., Pedemonte, Marina, Tacchetti, Paola, Lanzillotta, Valentina, Trucco, Federica, D’Amico, Adele, Bertini, Enrico, Astrea, Guja, Politano, Luisa, Masson, Riccardo, Baranello, Giovanni, Albamonte, Emilio, De Mattia, Elisa, Rao, Fabrizio, Sansone, Valeria A., Previtali, Stefano, Messina, Sonia, Vita, Gian Luca, Berardinelli, Angela, Mongini, Tiziana, Pini, Antonella, Pane, Marika, Mercuri, Eugenio, Vianello, Andrea, Bruno, Claudio, Hoffman, Eric P., Morgenroth, Lauren, Gordish‐Dressman, Heather, McDonald, Craig M., Pegoraro, Elena
Format: Artigo
Langue:Inglês
Publié: John Wiley and Sons Inc. 2020
Sujets:
Research Articles
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC7261745/
https://ncbi.nlm.nih.gov/pubmed/32343055
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51046
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