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Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduria.

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Title: Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduria.
Authors: Wongkittichote P; Children's National Rare Disease Institute, Children's National Health System, Washington DC 20010, United States; Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand; Department of Pediatrics, St. Louis Children's Hospital, Washington University School of Medicine, St. Louis, MO, USA., Cunningham G; Children's National Rare Disease Institute, Children's National Health System, Washington DC 20010, United States., Summar ML; Children's National Rare Disease Institute, Children's National Health System, Washington DC 20010, United States., Pumbo E; Children's National Rare Disease Institute, Children's National Health System, Washington DC 20010, United States., Forny P; Division of Metabolism, the Children's Research Center, The Swiss Newborn Screening Laboratory, University Children's Hospital Zurich, 8032 Zurich, Switzerland; The radiz-Rare Disease Initiative Zurich, Clinical Research Priority Program for Rare Diseases, the Center for Integrative Human Physiology, University of Zurich, 8006 Zurich, Switzerland., Baumgartner MR; Division of Metabolism, the Children's Research Center, The Swiss Newborn Screening Laboratory, University Children's Hospital Zurich, 8032 Zurich, Switzerland; The radiz-Rare Disease Initiative Zurich, Clinical Research Priority Program for Rare Diseases, the Center for Integrative Human Physiology, University of Zurich, 8006 Zurich, Switzerland., Chapman KA; Children's National Rare Disease Institute, Children's National Health System, Washington DC 20010, United States. Electronic address: KChapman@childrensnational.org.
Source: Molecular genetics and metabolism [Mol Genet Metab] 2019 Dec; Vol. 128 (4), pp. 444-451. Date of Electronic Publication: 2019 Oct 17.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE
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  Data: Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduria.
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  Data: <searchLink fieldCode="AU" term="%22Wongkittichote+P%22">Wongkittichote P</searchLink>; Children's National Rare Disease Institute, Children's National Health System, Washington DC 20010, United States; Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand; Department of Pediatrics, St. Louis Children's Hospital, Washington University School of Medicine, St. Louis, MO, USA.<br /><searchLink fieldCode="AU" term="%22Cunningham+G%22">Cunningham G</searchLink>; Children's National Rare Disease Institute, Children's National Health System, Washington DC 20010, United States.<br /><searchLink fieldCode="AU" term="%22Summar+ML%22">Summar ML</searchLink>; Children's National Rare Disease Institute, Children's National Health System, Washington DC 20010, United States.<br /><searchLink fieldCode="AU" term="%22Pumbo+E%22">Pumbo E</searchLink>; Children's National Rare Disease Institute, Children's National Health System, Washington DC 20010, United States.<br /><searchLink fieldCode="AU" term="%22Forny+P%22">Forny P</searchLink>; Division of Metabolism, the Children's Research Center, The Swiss Newborn Screening Laboratory, University Children's Hospital Zurich, 8032 Zurich, Switzerland; The radiz-Rare Disease Initiative Zurich, Clinical Research Priority Program for Rare Diseases, the Center for Integrative Human Physiology, University of Zurich, 8006 Zurich, Switzerland.<br /><searchLink fieldCode="AU" term="%22Baumgartner+MR%22">Baumgartner MR</searchLink>; Division of Metabolism, the Children's Research Center, The Swiss Newborn Screening Laboratory, University Children's Hospital Zurich, 8032 Zurich, Switzerland; The radiz-Rare Disease Initiative Zurich, Clinical Research Priority Program for Rare Diseases, the Center for Integrative Human Physiology, University of Zurich, 8006 Zurich, Switzerland.<br /><searchLink fieldCode="AU" term="%22Chapman+KA%22">Chapman KA</searchLink>; Children's National Rare Disease Institute, Children's National Health System, Washington DC 20010, United States. Electronic address: KChapman@childrensnational.org.
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  Data: <searchLink fieldCode="JN" term="%229805456%22">Molecular genetics and metabolism</searchLink> [Mol Genet Metab] 2019 Dec; Vol. 128 (4), pp. 444-451. <i>Date of Electronic Publication: </i>2019 Oct 17.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Academic+Press%22">Academic Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9805456 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1096-7206 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210967192%22">10967192 </searchLink><i>NLM ISO Abbreviation: </i>Mol Genet Metab <i>Subsets: </i>MEDLINE
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        Value: 10.1016/j.ymgme.2019.10.007
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      – TitleFull: Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduria.
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              Text: 2019 Dec
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