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Expanding the clinical spectrum of primary coenzyme Q10 deficiency type 6: The first case with cardiomyopathy.

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Title: Expanding the clinical spectrum of primary coenzyme Q10 deficiency type 6: The first case with cardiomyopathy.
Authors: Leeuwen L; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Lubout CMA; Department of Pediatrics, Section of Metabolic Diseases, University of Groningen, Groningen, The Netherlands., Nijenhuis HP; Department of Pediatrics, Center for Congenital Heart Diseases, University of Groningen, Groningen, The Netherlands., Meiners LC; Department of Radiology, University of Groningen, Groningen, The Netherlands., Vos YJ; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Herkert JC; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Source: Clinical genetics [Clin Genet] 2022 Oct; Vol. 102 (4), pp. 350-351. Date of Electronic Publication: 2022 Jul 06.
Publication Type: Case Reports; Letter
Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Expanding the clinical spectrum of primary coenzyme Q10 deficiency type 6: The first case with cardiomyopathy.
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  Data: <searchLink fieldCode="AU" term="%22Leeuwen+L%22">Leeuwen L</searchLink>; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Lubout+CMA%22">Lubout CMA</searchLink>; Department of Pediatrics, Section of Metabolic Diseases, University of Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Nijenhuis+HP%22">Nijenhuis HP</searchLink>; Department of Pediatrics, Center for Congenital Heart Diseases, University of Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Meiners+LC%22">Meiners LC</searchLink>; Department of Radiology, University of Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Vos+YJ%22">Vos YJ</searchLink>; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Herkert+JC%22">Herkert JC</searchLink>; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
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  Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2022 Oct; Vol. 102 (4), pp. 350-351. <i>Date of Electronic Publication: </i>2022 Jul 06.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1399-0004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1111/cge.14182
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              Text: 2022 Oct
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