Chargement en cours...
GEMINs: potential therapeutic targets for spinal muscular atrophy?
The motor neuron degenerative disease spinal muscular atrophy (SMA) remains one of the most frequently inherited causes of infant mortality. Afflicted patients loose the survival motor neuron 1 (SMN1) gene but retain one or more copies of SMN2, a homolog that is incorrectly spliced. Primary treatmen...
Enregistré dans:
| Auteurs principaux: | , |
|---|---|
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Frontiers Media S.A.
2014
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4197776/ https://ncbi.nlm.nih.gov/pubmed/25360080 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2014.00325 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|