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

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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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PubType: Academic Journal
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  Data: Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.
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  Data: <searchLink fieldCode="AU" term="%22Peng+Y%22">Peng Y</searchLink><br /><searchLink fieldCode="AU" term="%22Shinde+DN%22">Shinde DN</searchLink><br /><searchLink fieldCode="AU" term="%22Alexander+Valencia+C%22">Alexander Valencia C</searchLink><br /><searchLink fieldCode="AU" term="%22Mo+JS%22">Mo JS</searchLink><br /><searchLink fieldCode="AU" term="%22Rosenfeld+J%22">Rosenfeld J</searchLink><br /><searchLink fieldCode="AU" term="%22Cho+MT%22">Cho MT</searchLink><br /><searchLink fieldCode="AU" term="%22Chamberlin+A%22">Chamberlin A</searchLink><br /><searchLink fieldCode="AU" term="%22Li+Z%22">Li Z</searchLink><br /><searchLink fieldCode="AU" term="%22Liu+J%22">Liu J</searchLink><br /><searchLink fieldCode="AU" term="%22Gui+B%22">Gui B</searchLink>
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  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2018 Jun 15; Vol. 27 (12), pp. 2224.
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  Data: Journal Article; Published Erratum
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>PubMed not MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=29554255
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    Identifiers:
      – Type: doi
        Value: 10.1093/hmg/ddy072
    Languages:
      – Code: eng
        Text: English
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        StartPage: 2224
    Titles:
      – TitleFull: Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.
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          Name:
            NameFull: Peng Y
      – PersonEntity:
          Name:
            NameFull: Shinde DN
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            NameFull: Alexander Valencia C
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            NameFull: Mo JS
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            NameFull: Rosenfeld J
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            NameFull: Cho MT
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            NameFull: Chamberlin A
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            NameFull: Li Z
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            NameFull: Liu J
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            NameFull: Gui B
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          Dates:
            – D: 15
              M: 06
              Text: 2018 Jun 15
              Type: published
              Y: 2018
          Identifiers:
            – Type: issn-electronic
              Value: 1460-2083
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            – Type: volume
              Value: 27
            – Type: issue
              Value: 12
          Titles:
            – TitleFull: Human molecular genetics
              Type: main
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