Early Findings in Neonatal Cases of RYR1–Related Congenital Myopathies

Ryanodine receptor type 1-related congenital myopathies are the most represented subgroup among congenital myopathies (CMs), typically presenting a central core or multiminicore muscle histopathology and high clinical heterogeneity. We evaluated a cohort of patients affected with Ryanodine receptor...

Descripción completa

Detalles Bibliográficos
Autores principales: Mauri, Eleonora, Piga, Daniela, Govoni, Alessandra, Brusa, Roberta, Pagliarani, Serena, Ripolone, Michela, Dilena, Robertino, Cinnante, Claudia, Sciacco, Monica, Cassandrini, Denise, Nigro, Vincenzo, Bresolin, Nereo, Corti, Stefania, Comi, Giacomo P., Magri, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273285/
https://www.ncbi.nlm.nih.gov/pubmed/34262519
http://dx.doi.org/10.3389/fneur.2021.664618

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273285/
https://www.ncbi.nlm.nih.gov/pubmed/34262519
http://dx.doi.org/10.3389/fneur.2021.664618

Ejemplares similares