Prion-like domain disease-causing mutations and misregulation of alternative splicing relevance in limb-girdle muscular dystrophy (LGMD) 1G

Detalles Bibliográficos
Autores principales: Batlle, Cristina, Ventura, Salvador
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Perspective
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749493/
https://www.ncbi.nlm.nih.gov/pubmed/32594036
http://dx.doi.org/10.4103/1673-5374.284988

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749493/
https://www.ncbi.nlm.nih.gov/pubmed/32594036
http://dx.doi.org/10.4103/1673-5374.284988

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