טוען...
Intron 7 conserved sequence elements regulate the splicing of the SMN genes
Proximal spinal muscular atrophy (SMA) is a neuromuscular disease caused by low levels of the survival motor neuron (SMN) protein. In humans there are two nearly identical SMN genes, SMN1 and SMN2. The SMN2 gene generates a truncated protein, due to a C to T nucleotide alteration in exon 7, which le...
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| Main Authors: | , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2009
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2891348/ https://ncbi.nlm.nih.gov/pubmed/19701774 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-009-0733-7 |
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