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Molecular Crosstalk Between Non-SMN-Related and SMN-Related Spinal Muscular Atrophy
Most cases of spinal muscular atrophy are caused by functional loss of the survival of motor neuron 1 (SMN1) gene, while less than 5% of cases are attributed to genes other than SMN. Mutations in LMNA, the lamin A/C encoding gene, cause an adult form of spinal muscular atrophy (SMA), and in our rece...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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SAGE Publications
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133067/ https://www.ncbi.nlm.nih.gov/pubmed/32285042 http://dx.doi.org/10.1177/2633105520914301 |