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Biallelic mutations in the ferredoxin reductase gene cause ..:
Peng, Yanyan
;
Shinde, Deepali N
;
Valencia, C Alexander
...
Human Molecular Genetics. 26 (2017) 24 - p. 4937-4950 , 2017
Link:
https://doi.org/10.1093/hmg/ddx377
RT Journal T1
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddx377&Exemplar=1&LAN=DE A1 Peng, Yanyan A1 Shinde, Deepali N A1 Valencia, C Alexander A1 Mo, Jun-Song A1 Rosenfeld, Jill A1 Truitt Cho, Megan A1 Chamberlin, Adam A1 Li, Zhuo A1 Liu, Jie A1 Gui, Baoheng A1 Brockhage, Rachel A1 Basinger, Alice A1 Alvarez-Leon, Brenda A1 Heydemann, Peter A1 Magoulas, Pilar L A1 Lewis, Andrea M A1 Scaglia, Fernando A1 Gril, Solange A1 Chong, Shuk Ching A1 Bower, Matthew A1 Monaghan, Kristin G A1 Willaert, Rebecca A1 Plona, Maria-Renee A1 Dineen, Rich A1 Milan, Francisca A1 Hoganson, George A1 Powis, Zoe A1 Helbig, Katherine L A1 Keller-Ramey, Jennifer A1 Harris, Belinda PB Oxford University Press (OUP) YR 2017 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 26 IS 24 SP 4937 OP 4950 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddx377 DO https://doi.org/10.1093/hmg/ddx377 SF ELIB - SuUB Bremen
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