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Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegias

Mechanisms by which long corticospinal axons degenerate in hereditary spastic paraplegia (HSP) are largely unknown. Here, we have generated induced pluripotent stem cells (iPSCs) from patients with two autosomal recessive forms of HSP, SPG15 and SPG48, which are caused by mutations in the ZFYVE26 an...

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Podrobná bibliografie
Vydáno v:Hum Mol Genet
Hlavní autoři: Denton, Kyle, Mou, Yongchao, Xu, Chong-Chong, Shah, Dhruvi, Chang, Jaerak, Blackstone, Craig, Li, Xue-Jun
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2018
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6031053/
https://ncbi.nlm.nih.gov/pubmed/29726929
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy156
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