A novel de novo mutation in the Cardiac RyanodineReceptor Gene RyR2 in a patient with concealed LongQT Syndrome

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RAMOĞLU M. G., UÇAR T., türkgenç b., YAKICIER M. C., ATALAY S., TUTAR H. E.

50th Annual Meeting of the Association for European Paediatric and Congenital Cardiology,Rome, Italy, June 1–4, 2016, 1 - 04 Haziran 2016

• Yayın Türü: Bildiri
• Ankara Üniversitesi Adresli: Evet