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Abnormal mitochondrial transport and morphology as early pathological changes in human models of spinal muscular atrophy

Spinal muscular atrophy (SMA), characterized by specific degeneration of spinal motor neurons, is caused by mutations in the survival of motor neuron 1, telomeric (SMN1) gene and subsequent decreased levels of functional SMN. How the deficiency of SMN, a ubiquitously expressed protein, leads to spin...

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Detalhes bibliográficos
Publicado no:Dis Model Mech
Main Authors: Xu, Chong-Chong, Denton, Kyle R., Wang, Zhi-Bo, Zhang, Xiaoqing, Li, Xue-Jun
Formato: Artigo
Idioma:Inglês
Publicado em: The Company of Biologists Ltd 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4728333/
https://ncbi.nlm.nih.gov/pubmed/26586529
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.021766
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