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25 years of the SMN genes: the Copernican revolution of spinal muscular atrophy
The new era of advanced therapies has influenced and changed the views and perspectives of a neuromuscular disease such as spinal muscular atrophy (SMA). Being an autosomal recessive motor neuron disorder, characterized by different degrees of muscle weakness, after 25 years of the discovery of the...
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| Опубликовано в: : | Acta Myol |
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| Главные авторы: | , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Pacini Editore Srl
2020
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7783429/ https://ncbi.nlm.nih.gov/pubmed/33458589 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.36185/2532-1900-037 |
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