Results 151 to 153 of about 3,708 (153)

CRISPR/Cas9-mediated exon inclusion in Lama2 gene alleviates dystrophic pathology in MDC1A mouse model

Neuromuscular Disorders, 2016
D. Kemaladewi, E. Hyatt, Z. Ivakine, R. Cohn   +3 more
openaire   +1 more source

LAMA2 gene mutations are cause of congenital and limb-girdle muscular dystrophies

2013
R. Del Bo, F. Magri, F. Fortunato, M.G. D’Angelo, M. Pane, F. Bianco, A. Govoni, S. Corti, E. Mercuri, N. Bresolin, M. Moggio, G.P. Comi   +11 more
openaire   +1 more source

Targeted next generation sequencing identifies a novel deletion in LAMA2 gene in a congenital muscular dystrophy patient

2014
Aneek Das Bhowmik, Matta, Divya, C.Sundaram, Shagun Aggarwal, Ashwin B. Dalal   +4 more
openaire   +1 more source