학술논문
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
Document Type
Article
Author
Peng, Y.; Valencia, C.A.; Mo, J.-S.; Li, Z.; Liu, J.; Gui, B.; Brockhage, R.; Huang, T.; Shinde, D.N.; Chamberlin, A.; Powis, Z.; Helbig, K.L.; Tang, S.; Rosenfeld, J.; Magoulas, P.L.; Lewis, A.M.; Scaglia, F.; Cho, M.T.; Monaghan, K.G.; Willaert, R.; Milan, F.; Keller-Ramey, J.; Basinger, A.; Alvarez-Leon, B.; Heydemann, P.; Gril, S.; Chong, S.C.; Bower, M.; Plona, M.-R.; Dineen, R.; Hoganson, G.; Harris, B.; Anderson, L.C.; Green, T.; Sukoff Rizzo, S.J.; Reinholdt, L.G.; Kaylor, J.; Sellars, E.; Chen, J.; Guan, M.-X.; Sparagana, S.P.; Gibson, J.B.
Source
In: Human Molecular Genetics . (Human Molecular Genetics, December 2017, 26(24):4937-4950)
Subject
Language
English
ISSN
14602083
09646906
09646906