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

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Bibliographic Details
Title: Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.
Authors: Peng Y, Shinde DN, Alexander Valencia C, Mo JS, Rosenfeld J, Cho MT, Chamberlin A, Li Z, Liu J, Gui B
Source: Human molecular genetics [Hum Mol Genet] 2018 Jun 15; Vol. 27 (12), pp. 2224.
Publication Type: Journal Article; Published Erratum
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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ISSN:1460-2083
DOI:10.1093/hmg/ddy072