Molecular and Histopathological Characterization of Patients Presenting with the Duchenne Muscular Dystrophy Phenotype in a Tertiary Care Center in Southern India

The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations

Catherine L. Bladen, David Salgado, Soledad Monges et al. · Human Mutation · 2015 · 744 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations

Mariko Okubo, Narihiro Minami, Kanako Goto et al. · Journal of Human Genetics · 2016 · 106 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

<i>DMD</i>exon 1 truncating point mutations: Amelioration of phenotype by alternative translation initiation in exon 6

Olga L. Gurvich, Baijayanta Maiti, Robert B. Weiss et al. · Human Mutation · 2009 · 69 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Proportion and pattern of dystrophin gene deletions in North Indian Duchenne and Becker muscular dystrophy patients

Vinita Singh, Shirish Sinha, Sudhish Mishra et al. · Human Genetics · 1997 · 40 citations

Life Sciences, Genetics, Molecular Genetics +12

Are there ethnic differences in deletions in the dystrophin gene?

Minakshi Banerjee, Ishwar C. Verma · American Journal of Medical Genetics · 1997 · 37 citations

Life Sciences, Genetics, Molecular Genetics +12