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

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:
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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author Peng, Yanyan
Shinde, Deepali N
Alexander Valencia, C
Mo, Jun-Song
Rosenfeld, Jill
Cho, Megan Truitt
Chamberlin, Adam
Li, Zhuo
Liu, Jie
Gui, Baoheng
author_facet Peng, Yanyan
Shinde, Deepali N
Alexander Valencia, C
Mo, Jun-Song
Rosenfeld, Jill
Cho, Megan Truitt
Chamberlin, Adam
Li, Zhuo
Liu, Jie
Gui, Baoheng
author_sort Peng, Yanyan
collection PubMed
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spelling pubmed-59857262018-06-06 Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy Peng, Yanyan Shinde, Deepali N Alexander Valencia, C Mo, Jun-Song Rosenfeld, Jill Cho, Megan Truitt Chamberlin, Adam Li, Zhuo Liu, Jie Gui, Baoheng Hum Mol Genet Corrigendum Oxford University Press 2018-06-15 2018-03-15 /pmc/articles/PMC5985726/ /pubmed/29554255 http://dx.doi.org/10.1093/hmg/ddy072 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Corrigendum
Peng, Yanyan
Shinde, Deepali N
Alexander Valencia, C
Mo, Jun-Song
Rosenfeld, Jill
Cho, Megan Truitt
Chamberlin, Adam
Li, Zhuo
Liu, Jie
Gui, Baoheng
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
title Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
title_full Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
title_fullStr Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
title_full_unstemmed Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
title_short Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
title_sort biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
topic Corrigendum
url 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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