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...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
SAGE Publishing
2020-03-01
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| Edice: | Neuroscience Insights |
| On-line přístup: | https://doi.org/10.1177/2633105520914301 |
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