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Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy

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Detalles Bibliográficos
Autores principales:	Peng, Yanyan, Shinde, Deepali N, Alexander Valencia, C, Mo, Jun-Song, Rosenfeld, Jill, Cho, Megan Truitt, Chamberlin, Adam, Li, Zhuo, Liu, Jie, Gui, Baoheng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2018
Materias:	Corrigendum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985726/ https://www.ncbi.nlm.nih.gov/pubmed/29554255 http://dx.doi.org/10.1093/hmg/ddy072

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