A Journey with LGMD: From Protein Abnormalities to Patient Impact

The limb-girdle muscular dystrophies (LGMD) are a collection of genetic diseases united in their phenotypical expression of pelvic and shoulder area weakness and wasting. More than 30 subtypes have been identified, five dominant and 26 recessive. The increase in the characterization of new genotypes...

Descripción completa

Detalles Bibliográficos
Autores principales: Georganopoulou, Dimitra G., Moisiadis, Vasilis G., Malik, Firhan A., Mohajer, Ali, Dashevsky, Tanya M., Wuu, Shirley T., Hu, Chih-Kao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190568/
https://www.ncbi.nlm.nih.gov/pubmed/34110586
http://dx.doi.org/10.1007/s10930-021-10006-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190568/
https://www.ncbi.nlm.nih.gov/pubmed/34110586
http://dx.doi.org/10.1007/s10930-021-10006-9

Ejemplares similares