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Miro1 deficiency in amyotrophic lateral sclerosis

Proper transportation of mitochondria to sites with high energy demands is critical for neuronal function and survival. Impaired mitochondrial movement has been repeatedly reported in motor neurons of amyotrophic lateral sclerosis (ALS) patients and indicated as an important mechanism contributing t...

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Detalles Bibliográficos
Publicado en:Front Aging Neurosci
Autores principales: Zhang, Fan, Wang, Wenzhang, Siedlak, Sandra L., Liu, Yingchao, Liu, Jun, Jiang, Keji, Perry, George, Zhu, Xiongwei, Wang, Xinglong
Formato: Artigo
Lenguaje:Inglês
Publicado: Frontiers Media S.A. 2015
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4443026/
https://ncbi.nlm.nih.gov/pubmed/26074815
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnagi.2015.00100
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