Flow diagram depicting the dystrophinopathy (DMD/BMD) and limb-girdle

Becker muscular dystrophy (Case 38) - Neuromuscular Disease

Diagnosing Muscular Dystrophies: Comparison of Techniques and Their Cost Effectiveness: A Multi-institutional Study - Journal of Neurosciences in Rural Practice

Miriam REYNA FABIAN, Researcher, Professor, Instituto Nacional de Pediatría, Mexico City, INP, Molecular Biology

PDF) 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

Practical approach to the genetic diagnosis of unsolved dystrophinopathies: a stepwise strategy in the genomic era

Hereditary and Acquired Types of Myopathy

Clinical and Molecular Diagnosis in Muscular Dystrophies

Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing, BMC Medical Genetics

Common recessive limb girdle muscular dystrophies ○ Until the publication of this article, 27 LGMD subtypes have been classified, and at least five additional e…

Matilde RUÍZ-GARCÍA, Head of Department, Instituto Nacional de Pediatría, Mexico City, INP, Department of Neurology

Muscle MRI and functional outcome measures in Becker muscular dystrophy

Surface ECG recordings on wt and dysf mice. A. Typical original ECG

PDF) Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling