M. G. RAMOĞLU Et Al. , "A novel de novo mutation in the Cardiac Ryanodine Gene (RyR2) in a patient with concealed Long QT Syndrome," 50th Annual Meeting of the Associationn for European Pediatric and Congenital Cardiology , vol.26, ROMA, Italy, pp.41-42, 2016
RAMOĞLU, M. G. Et Al. 2016. A novel de novo mutation in the Cardiac Ryanodine Gene (RyR2) in a patient with concealed Long QT Syndrome. 50th Annual Meeting of the Associationn for European Pediatric and Congenital Cardiology , (ROMA, Italy), 41-42.
RAMOĞLU, M. G., UÇAR, T., TÜRKGENÇ, B., ATALAY, S., & TUTAR, H. E., (2016). A novel de novo mutation in the Cardiac Ryanodine Gene (RyR2) in a patient with concealed Long QT Syndrome . 50th Annual Meeting of the Associationn for European Pediatric and Congenital Cardiology (pp.41-42). ROMA, Italy
RAMOĞLU, MEHMET Et Al. "A novel de novo mutation in the Cardiac Ryanodine Gene (RyR2) in a patient with concealed Long QT Syndrome," 50th Annual Meeting of the Associationn for European Pediatric and Congenital Cardiology, ROMA, Italy, 2016
RAMOĞLU, MEHMET G. Et Al. "A novel de novo mutation in the Cardiac Ryanodine Gene (RyR2) in a patient with concealed Long QT Syndrome." 50th Annual Meeting of the Associationn for European Pediatric and Congenital Cardiology , ROMA, Italy, pp.41-42, 2016
RAMOĞLU, M. G. Et Al. (2016) . "A novel de novo mutation in the Cardiac Ryanodine Gene (RyR2) in a patient with concealed Long QT Syndrome." 50th Annual Meeting of the Associationn for European Pediatric and Congenital Cardiology , ROMA, Italy, pp.41-42.
@conferencepaper{conferencepaper, author={MEHMET GÖKHAN RAMOĞLU Et Al. }, title={A novel de novo mutation in the Cardiac Ryanodine Gene (RyR2) in a patient with concealed Long QT Syndrome}, congress name={50th Annual Meeting of the Associationn for European Pediatric and Congenital Cardiology}, city={ROMA}, country={Italy}, year={2016}, pages={41-42} }