PRKAG2Protein Kinase, Amp-Activated, Noncatalytic, Gamma2
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In addition, 5/7 PPAR signaling genes (solute carrier family 27 (fatty acid transporter), member 6 (SLC27A6), carnitine palmitoyltransferase 2 (CPT2), SORBS1, phosphoenolpyruvate carboxykinase 1 (PCK1) and SLC27A1) and 4 adipocytokine signaling pathway genes (OB, PRKAG2, PCK1, and PPARGC1A) were upregulated in the H group, which are significant to the development of marbling.
Genetic HCM ARVC/D LV noncompaction Storage diseases PRKAG2 Danon Conduction defects Mitochondrial myopathies Ion-channel disorders Long QT syndrome Short QT syndrome Brugada syndrome Catecholaminergic polymorphic ventricular tachycardia Asian sudden unexplained nocturnal death syndrome Acquired Inflammatory (myocarditis) Stress provoked (Takotsubo) Peripartum Tachycardia induced Infants of IDDM mothers Mixed Dilated cardiomyopathy Restrictive (nonhypertrophied and nondilated) Table 3.
La Forma familiar se hereda como un rasgo genetico autosomico dominante y se ha relacionado con el gen PRKAG2.