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Calcium is reduced in presynaptic mitochondria of motor nerve terminals during neurotransmission in SMA mice
Spinal muscular atrophy (SMA) is an autosomal recessive degenerative motor neuron disease characterized by symmetrical muscle weakness and atrophy of limb and trunk muscles being the most severe genetic disease in children. In SMA mouse models, motor nerve terminals display neurotransmitter release...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127408/ https://www.ncbi.nlm.nih.gov/pubmed/33693569 http://dx.doi.org/10.1093/hmg/ddab065 |