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

Yanyan Peng | Zendy; Deepali N. Shinde | Zendy; C. Alexander Valencia | Zendy; Jun-Song Mo | Zendy; Jill A. Rosenfeld | Zendy; Megan Truitt Cho | Zendy; Adam Chamberlin | Zendy; Zhuo Li | Zendy; Jie Liu | Zendy; Baoheng Gui | Zendy

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

Author(s) -

Yanyan Peng,

Deepali N. Shinde,

C. Alexander Valencia,

Jun-Song Mo,

Jill A. Rosenfeld,

Megan Truitt Cho,

Adam Chamberlin,

Zhuo Li,

Jie Liu,

Baoheng Gui

Publication year - 2018

Publication title -

human molecular genetics

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.811

H-Index - 276

eISSN - 1460-2083

pISSN - 0964-6906

DOI - 10.1093/hmg/ddy072

Subject(s) - biology , ferredoxin , gene , genetics , atrophy , ferredoxin—nadp(+) reductase , reductase , mutation , enzyme , biochemistry

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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