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A survey of transcripts generated by spinal muscular atrophy genes
Human Survival Motor Neuron (SMN) genes code for SMN, an essential multifunctional protein. Complete loss of SMN is embryonic lethal, while low levels of SMN lead to spinal muscular atrophy (SMA), a major genetic disease of children and infants. Reduced levels of SMN are associated with the abnormal...
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| Опубликовано в: : | Biochim Biophys Acta Gene Regul Mech |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2020
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7302838/ https://ncbi.nlm.nih.gov/pubmed/32387331 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbagrm.2020.194562 |
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