RAMOĞLU, M. G. Et Al. 2016. A novel de novo mutation in the Cardiac RyanodineReceptor Gene RyR2 in a patient with concealed LongQT Syndrome. 50th Annual Meeting of the Association for European Paediatric and Congenital Cardiology,Rome, Italy, June 1–4, 2016 .

RAMOĞLU, M. G., UÇAR, T., türkgenç, b., YAKICIER, M. C., ATALAY, S., & TUTAR, H. E., (2016). A novel de novo mutation in the Cardiac RyanodineReceptor Gene RyR2 in a patient with concealed LongQT Syndrome . 50th Annual Meeting of the Association for European Paediatric and Congenital Cardiology,Rome, Italy, June 1–4, 2016

RAMOĞLU, MEHMET Et Al. "A novel de novo mutation in the Cardiac RyanodineReceptor Gene RyR2 in a patient with concealed LongQT Syndrome," 50th Annual Meeting of the Association for European Paediatric and Congenital Cardiology,Rome, Italy, June 1–4, 2016, 2016

RAMOĞLU, MEHMET G. Et Al. "A novel de novo mutation in the Cardiac RyanodineReceptor Gene RyR2 in a patient with concealed LongQT Syndrome." 50th Annual Meeting of the Association for European Paediatric and Congenital Cardiology,Rome, Italy, June 1–4, 2016 , 2016

RAMOĞLU, M. G. Et Al. (2016) . "A novel de novo mutation in the Cardiac RyanodineReceptor Gene RyR2 in a patient with concealed LongQT Syndrome." 50th Annual Meeting of the Association for European Paediatric and Congenital Cardiology,Rome, Italy, June 1–4, 2016 .

@conferencepaper{conferencepaper, author={MEHMET GÖKHAN RAMOĞLU Et Al. }, title={A novel de novo mutation in the Cardiac RyanodineReceptor Gene RyR2 in a patient with concealed LongQT Syndrome}, congress name={50th Annual Meeting of the Association for European Paediatric and Congenital Cardiology,Rome, Italy, June 1–4, 2016}, city={}, country={}, year={2016}}