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25 years of the SMN genes: the Copernican revolution of spinal muscular atrophy
The new era of advanced therapies has influenced and changed the views and perspectives of a neuromuscular disease such as spinal muscular atrophy (SMA). Being an autosomal recessive motor neuron disorder, characterized by different degrees of muscle weakness, after 25 years of the discovery of the...
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| Gepubliceerd in: | Acta Myol |
|---|---|
| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Pacini Editore Srl
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7783429/ https://ncbi.nlm.nih.gov/pubmed/33458589 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.36185/2532-1900-037 |
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