Lataa...
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...
Tallennettuna:
| Julkaisussa: | Front Physiol |
|---|---|
| Päätekijä: | |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2020
|
| Aiheet: | |
| Linkit: | 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 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|