Genetics Archives • World Duchenne

Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy

Naidoo M, Anthony K. Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy. Molecular neurobiology 2020;57:1748-1767 Abstract Duchenne muscular…

Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophies

Ling C, Dai Y, Fang L, et al. Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and…

Longitudinal serum biomarker screening identifies malate dehydrogenase 2 as candidate prognostic biomarker for Duchenne muscular dystrophy

Signorelli M, Ayoglu B, Johansson C, et al. Longitudinal serum biomarker screening identifies malate dehydrogenase 2 as candidate prognostic biomarker…

TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy

Spitali P, Zaharieva I, Bohringer S, et al. TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy.…

Becker muscular dystrophy caused by exon 2-truncating mutation of DMD.

Ikeda T, Fujinaka H, Goto K, Nakajima T, Ozawa T. Becker muscular dystrophy caused by exon 2-truncating mutation of DMD.…

Predominance of Dystrophinopathy Genotypes in Mexican Male Patients Presenting as Muscular Dystrophy with A Normal Multiplex Polymerase Chain Reaction DMD Gene Result: A Study Including Targeted Next-Generation Sequencing

Alcantara-Ortigoza MA, Reyna-Fabian ME, Gonzalez-Del Angel A, et al. Predominance of Dystrophinopathy Genotypes in Mexican Male Patients Presenting as Muscular…

Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center

Zhang J, Ma D, Liu G, et al. Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies…

Breakpoint junction features of seven DMD deletion mutations

Keegan NP, Wilton SD, Fletcher S. Breakpoint junction features of seven DMD deletion mutations. Human genome variation 2019;6:39 Abstract…

Large in-frame 5' deletions in DMD associated with mild Duchenne muscular dystrophy: Two case reports and a review of the literature

Gibbs EM, Barthelemy F, Douine ED, et al. Large in-frame 5' deletions in DMD associated with mild Duchenne muscular dystrophy:…

The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: the era of personalized medicine

Iskandar K, Dwianingsih EK, Pratiwi L, et al. The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD…

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Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy

Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophies

Longitudinal serum biomarker screening identifies malate dehydrogenase 2 as candidate prognostic biomarker for Duchenne muscular dystrophy

TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy

Becker muscular dystrophy caused by exon 2-truncating mutation of DMD.

Predominance of Dystrophinopathy Genotypes in Mexican Male Patients Presenting as Muscular Dystrophy with A Normal Multiplex Polymerase Chain Reaction DMD Gene Result: A Study Including Targeted Next-Generation Sequencing

Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center

Breakpoint junction features of seven DMD deletion mutations

Large in-frame 5' deletions in DMD associated with mild Duchenne muscular dystrophy: Two case reports and a review of the literature

The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: the era of personalized medicine

World Duchenne Organization announces Accredited Duchenne Centers Program

Official WDAD2022 Event: Women and Duchenne

World Duchenne Organization Leadership Award for Professor Muntoni