Dp412e: a novel human embryonic dystrophin isoform induced by BMP4 in early differentiated cells.
Fiche publication
Date publication
janvier 2015
Journal
Skeletal muscle
Auteurs
Membres identifiés du Cancéropôle Est :
Pr CHELLY Jamel
Tous les auteurs :
Massouridès E, Polentes J, Mangeot PE, Mournetas V, Nectoux J, Deburgrave N, Nusbaum P, Leturcq F, Popplewell L, Dickson G, Wein N, Flanigan KM, Peschanski M, Chelly J, Pinset C
Lien Pubmed
Résumé
Duchenne muscular dystrophy (DMD) is a devastating X-linked recessive genetic myopathy. DMD physiopathology is still not fully understood and a prenatal onset is suspected but difficult to address.
Référence
Skelet Muscle. 2015 ;5:40