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pro vyhledávání: '"José-Alain Sahel"'
Autor:
Hélène Cwerman-Thibault, Sébastien Augustin, Christophe Lechauve, Jessica Ayache, Sami Ellouze, José-Alain Sahel, Marisol Corral-Debrinski
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 2, Iss , Pp - (2015)
Leber hereditary optic neuropathy is due to mitochondrial DNA mutations; in â¼70% of all cases, a point mutation in the mitochondrial NADH dehydrogenase subunit 4, ND4, gene leads to central vision loss. We optimized allotopic expression (nuclear t
Externí odkaz:
https://doaj.org/article/ab38167873024ae38c387883197886b4
Publikováno v:
Fair Disclosure Wire (Quarterly Earnings Reports). 01/06/2021.