Cargando…
Genetic diagnosis as a tool for personalized treatment of Duchenne muscular dystrophy
Accurate definition of genetic mutations causing Duchenne muscular dystrophy (DMD) has always been relevant in order to provide genetic counseling to patients and families, and helps to establish the prognosis in the case where the distinction between Duchenne, Becker, or intermediate muscular dystr...
Autores principales: | Bello, Luca, Pegoraro, Elena |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pacini Editore SRL
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5416739/ https://www.ncbi.nlm.nih.gov/pubmed/28484312 |
Ejemplares similares
-
The “Usual Suspects”: Genes for Inflammation, Fibrosis, Regeneration, and Muscle Strength Modify Duchenne Muscular Dystrophy
por: Bello, Luca, et al.
Publicado: (2019) -
Therapeutic opportunities and clinical outcome measures in Duchenne muscular dystrophy
por: Ricci, Giulia, et al.
Publicado: (2022) -
Teaching an Old Molecule New Tricks: Drug Repositioning for Duchenne Muscular Dystrophy
por: Vitiello, Libero, et al.
Publicado: (2019) -
Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy
por: Hogarth, Marshall W., et al.
Publicado: (2017) -
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy
por: Barp, Andrea, et al.
Publicado: (2015)