Carregant...
Zebrafish Models of LAMA2-Related Congenital Muscular Dystrophy (MDC1A)
LAMA2-related congenital muscular dystrophy (CMD; LAMA2-MD), also referred to as merosin deficient CMD (MDC1A), is a severe neonatal onset muscle disease caused by recessive mutations in the LAMA2 gene. LAMA2 encodes laminin α2, a subunit of the extracellular matrix (ECM) oligomer laminin 211. There...
Guardat en:
| Publicat a: | Front Mol Neurosci |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2020
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7364686/ https://ncbi.nlm.nih.gov/pubmed/32742259 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2020.00122 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|