Associated Papers
Theragnosis for Duchenne Muscular Dystrophy.
Luce L et al.
Frontiers in Pharmacology, 2021
Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan.
Okubo M et al.
Orphanet Journal of Rare Diseases, 2017
28859693 (PubMed )
Supplement: 13023_2017_703_MOESM1_ESM.pdf
Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy.
Rani AQ et al.
Journal of Neurogenetics, 2013
Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy.
Marini M et al.
The Medical Journal of Malaysia, 2008
Select a paper to view details