Limb - girdle muscular dystrophy type 2A with normal Calpain - 3 expression caused by a homozygous mutation in CAPN3 gene: one case report.
| Publicado en: | Chinese Journal of Contemporary Neurology & Neurosurgery Vol. 25; no. 11; pp. 1040 - 1046 |
|---|---|
| Autores principales: | , , , , , |
| Formato: | case study pictorial tables/charts Journal Article |
| Publicado: |
Chinese Journal of Contemporary Neurology & Neurosurgery
Nov2025
|
| Acceso en línea: | Ver este registro en EBSCOhost |