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Mechanism of Splicing Regulation of Spinal Muscular Atrophy Genes
Spinal muscular atrophy (SMA) is one of the major genetic disorders associated with infant mortality. More than 90% cases of SMA result from deletions or mutations of Survival Motor Neuron 1 (SMN1) gene. SMN2, a nearly identical copy of SMN1, does not compensate for the loss of SMN1 due to predomina...
Shranjeno v:
| izdano v: | Adv Neurobiol |
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| Main Authors: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2018
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6026014/ https://ncbi.nlm.nih.gov/pubmed/29916015 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-3-319-89689-2_2 |
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