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ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins (vol 27, pg 2739, 2018)

机译:患有婴儿发病的患者的患者中的ISCA1突变导致线粒体[4FE-4S]蛋白质中的缺陷(Vol 27,PG 2739,2018)

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  • 来源
    《Human Molecular Genetics》 |2018年第20期|共1页
  • 作者单位

    Bambino Gesu Pediat Hosp IRCCS Unit Muscular &

    Neurodegenerat Disorders Lab Mol Med Viale San;

    Philipps Univ Marburg Inst Zytobiol Marburg Germany;

    Philipps Univ Marburg Inst Zytobiol Marburg Germany;

    Philipps Univ Marburg Inst Zytobiol Marburg Germany;

    Natl Res Council CNR Inst Biomembrane Bioenerget &

    Mol Biotechnol IBIO Bari Italy;

    Univ Bari Dept Biosci Biotechnol &

    Biopharmaceut Lab Biochem &

    Mol Biol Bari Italy;

    Bambino Gesu Pediat Hosp IRCCS Unit Muscular &

    Neurodegenerat Disorders Lab Mol Med Viale San;

    Bambino Gesu Pediat Hosp IRCCS Unit Muscular &

    Neurodegenerat Disorders Lab Mol Med Viale San;

    Univ Bari Dept Biosci Biotechnol &

    Biopharmaceut Lab Biochem &

    Mol Biol Bari Italy;

    Bambino Gesu Pediat Hosp IRCCS Unit Muscular &

    Neurodegenerat Disorders Lab Mol Med Viale San;

    Bambino Gesu Pediat Hosp IRCCS Unit Muscular &

    Neurodegenerat Disorders Lab Mol Med Viale San;

    Bambino Gesu Pediat Hosp IRCCS Div Metab Rome Italy;

    Bambino Gesu Pediat Hosp IRCCS Unit Muscular &

    Neurodegenerat Disorders Lab Mol Med Viale San;

    Bambino Gesu Pediat Hosp IRCCS Div Metab Rome Italy;

    Bambino Gesu Pediat Hosp IRCCS Unit Muscular &

    Neurodegenerat Disorders Lab Mol Med Viale San;

    Philipps Univ Marburg Inst Zytobiol Marburg Germany;

    Bambino Gesu Pediat Hosp IRCCS Unit Muscular &

    Neurodegenerat Disorders Lab Mol Med Viale San;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医学遗传学;
  • 关键词

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