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Neuromuscular Junctions as Key Contributors and Therapeutic Targets in Spinal Muscular Atrophy

Spinal muscular atrophy (SMA) is a recessive autosomal neuromuscular disease, representing the most common fatal pediatric pathology. Even though, classically and in a simplistic way, it is categorized as a motor neuron (MN) disease, there is an increasing general consensus that its pathogenesis is...

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Bibliografische gegevens
Gepubliceerd in:Front Neuroanat
Hoofdauteurs: Boido, Marina, Vercelli, Alessandro
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Frontiers Media S.A. 2016
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4737916/
https://ncbi.nlm.nih.gov/pubmed/26869891
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnana.2016.00006
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