PTEN Inhibition Ameliorates Muscle Degeneration and Improves Muscle Function in a Mouse Model of Duchenne Muscular Dystrophy: Molecular Therapy
Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies | SpringerLink
The importance of genetic diagnosis for Duchenne muscular dystrophy | Journal of Medical Genetics
CRISPR technologies for the treatment of Duchenne muscular dystrophy: Molecular Therapy
Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies | SpringerLink
Muscular dystrophies - The Lancet
JCM | Free Full-Text | Innovative Therapeutic Approaches for Duchenne Muscular Dystrophy
Duchenne Muscular Dystrophy, DMD - The Medical Biochemistry Page
Overview of the genetic diagnosis based on the neurological panel results | Download Table
Matrilineal analysis of mutations in the DMD gene in a multigenerational South Indian cohort using DMD gene panel sequencing - Shastry - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
FDA panel votes down Sarepta drug for Duchenne muscular dystrophy
EMQN best practice guidelines for genetic testing in dystrophinopathies | European Journal of Human Genetics
Guidelines for genetic testing of muscle and neuromuscular junction disorders - Nicolau - 2021 - Muscle & Nerve - Wiley Online Library
Cardiac Myoediting Attenuates Cardiac Abnormalities in Human and Mouse Models of Duchenne Muscular Dystrophy | Circulation Research
Comprehensive Mutation Analysis for Congenital Muscular Dystrophy: A Clinical PCR-Based Enrichment and Next-Generation Sequencing Panel | PLOS ONE
Patients presenting with features of muscular dystrophy (42). BMD,... | Download Scientific Diagram
Genetic Testing For FSHD Diagnosis | FSHD Society
PGD for Duchenne muscular dystrophy (DMD)
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management - The Lancet Neurology
The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease | Orphanet Journal of Rare Diseases | Full Text
Learn How to Understand Genetic Test Results | EXONDYS 51 (eteplirsen) injection | EXONDYS 51
Clinical utility of multigene analysis in over 25,000 patients with neuromuscular disorders | Neurology Genetics
Evaluating the potential of novel genetic approaches for the treatment of Duchenne muscular dystrophy | European Journal of Human Genetics
Molecular and Histopathological Characterization of Patients Presenting with the Duchenne Muscular Dystrophy Phenotype in a Tertiary Care Center in Southern India
What is Muscular Dystrophy Gene Panel ?
Dystrophin
