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26 Possible Causes for Mutation in the Glycerol-3-Phosphate Dehydrogenase 1 Gene

  • Cardiac Arrhythmia

    Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na current and causes inherited arrhythmias.[ncbi.nlm.nih.gov]

  • Brugada Syndrome

    Mutations in Glycerol-3-phosphate dehydrogenase 1-like (GPD1L) gene are also seen in some patients of Brugada syndrome.[symptoma.com] The gene was recently identified in a preliminary report as the glycerol-3-phosphate dehydrogenase 1-like gene, and the mutation in glycerol-3-phosphate dehydrogenase 1-like[dx.doi.org] Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na current and causes inherited arrhythmias.[ncbi.nlm.nih.gov]

  • Hypertrophic Cardiomyopathy

    Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na   current and causes inherited arrhythmias. Circulation. 2007;116:2260–8.[doi.org] Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome. Circ Arrhythm Electrophysiol. 2008;1:209–18. PubMed CrossRef Google Scholar 60.[doi.org]

  • Lenegre Disease

    Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome.[nature.com] Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na current and causes inherited arrhythmias. Circulation 2007; 116 : 2260–2268. 36.[nature.com] Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans. J Clin Invest 2008; 118 : 2260–2268. 37.[nature.com]

  • Catecholaminergic Polymorphic Ventricular Tachycardia

    Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na current and causes inherited arrhythmias. Circulation. 2007 ; 116 :2260–2268.[dx.doi.org]

  • Familial Short QT Syndrome

    A mutation in the glycerol-3-phosphate dehydrogenase 1-like gene (GPD1L) causes Brugada syndrome. Heart Rhythm. 2006 ; 3 : S32. Abstract. Google Scholar[doi.org] The gene was recently identified as the Glycerol-3-Phosphate Dehydrogenase 1-Like Gene ( GPD1L ).[af-ablation.org] A mutation in GPD1L has been shown to result in a partial reduction of I Na Knowledge thus far gained through genetic analysis suggests that identification of specific mutations[af-ablation.org]

  • Long QT Syndrome 3

    Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na current and causes inherited arrhythmias.[emedicine.medscape.com]

  • Sudden Cardiac Death

    Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na current and causes inherited arrhythmias. Circulation. 2007;116(20):2260–8.[jbiomedsci.biomedcentral.com]

  • Bjornstad Syndrome

    Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na current and causes inherited arrhythmias.[emedicine.medscape.com]

  • Sudden Infant Death Syndrome

    Recently, a genome-wide linkage study involving a large pedigree with BrS phenotype revealed that the glycerol-3-phosphate dehydrogenase 1–like gene ( GPD1-L ) is associated[circ.ahajournals.org] Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome .[nature.com] 1 like gene (GPD1-L) mutations in sudden infant death syndrome.[doi.org]

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