Fingerprint
Dive into the research topics of 'Severe congenital muscular dystrophy in a Mexican family with a new nonsense mutation (R2578X) in the laminin α-2 gene'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Severe congenital muscular dystrophy in a Mexican family with a new nonsense mutation (R2578X) in the laminin α-2 gene
Ramon M. Coral-Vazquez, Haydee Rosas-Vargas, Pedro Meza-Espinosa, Irma Mendoza, Juan C. Huicochea, Guillermo Ramon, Fabio Salamanca
Research output: Contribution to journal › Article › peer-review
8
Scopus
citations