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Cardiovascular involvement in later-onset malonyl-CoA decarboxylase deficiency: Case studies and literature review.
Monda, Emanuele; Bakalakos, Athanasios; Syrris, Petros; Mohiddin, Saidi; Ferdinandusse, Sacha; Murphy, Elaine; Elliott, Perry Mark.
Affiliation
  • Monda E; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy; Institute of Cardiovascular Science, University College of London, London, UK. Electronic address: emanuelemonda@me.com.
  • Bakalakos A; Institute of Cardiovascular Science, University College of London, London, UK.
  • Syrris P; Institute of Cardiovascular Science, University College of London, London, UK.
  • Mohiddin S; Barts Health NHS Trust, London, UK; Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Ferdinandusse S; Laboratory Genetic Metabolic Diseases, Department of Clinical Chemistry, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
  • Murphy E; Charles Dent Metabolic Unit, The National Hospital for Neurology and Neurosurgery, London, UK.
  • Elliott PM; Institute of Cardiovascular Science, University College of London, London, UK; Barts Health NHS Trust, London, UK.
Eur J Med Genet ; 66(12): 104885, 2023 Dec.
Article in En | MEDLINE | ID: mdl-37979716

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Hypertrophic / Cardiomyopathy, Dilated / Metabolism, Inborn Errors Limits: Adult / Humans / Infant / Male Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2023 Document type: Article Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Hypertrophic / Cardiomyopathy, Dilated / Metabolism, Inborn Errors Limits: Adult / Humans / Infant / Male Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2023 Document type: Article Country of publication: Netherlands