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Mitofusin 2 Dysfunction and Disease in Mice and Men
A causal relationship between Mitofusin (MFN) 2 gene mutations and the hereditary axonal neuropathy Charcot-Marie-Tooth disease type 2A (CMT2A) was described over 15 years ago. During the intervening period much has been learned about MFN2 functioning in mitochondrial fusion, calcium signaling, and...
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| Опубликовано в: : | Front Physiol |
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| Главный автор: | |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Frontiers Media S.A.
2020
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7363930/ https://ncbi.nlm.nih.gov/pubmed/32733278 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2020.00782 |
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