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. 2018 Mar 15;27(12):2224. doi: 10.1093/hmg/ddy072

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

Yanyan Peng, Deepali N Shinde, C Alexander Valencia, Jun-Song Mo, Jill Rosenfeld, Megan Truitt Cho, Adam Chamberlin, Zhuo Li, Jie Liu, Baoheng Gui
PMCID: PMC5985726  PMID: 29554255

Human Molecular Genetics, 2017, 26(24), 4937–4950.

doi: 10.1093/hmg/ddx377

The authors regret the following errors in the above paper: in Figure 1 on page 4939, the mutation in Family 7 originally read as ‘c.613A>G’ instead of ‘c.631A>G’, and for Family 10, ‘c.1228C>T’ instead of ‘c.1226C>T’.  In addition, there was a discrepancy for Family 8 between Figure 1 and Table 1; the affected individuals in Figure 1 were listed as ‘c.472G>A, c.637A>T; p.V158M, p.I213F’ instead of ‘c.1120G>A p.D374N’ as in Table 1. These errors have now been corrected in the online version of the paper.


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