AKGÜN DOĞAN, Ö. Et Al. 2022. Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1. JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY , vol.33, no.2 , 262-273.

AKGÜN DOĞAN, Ö., Agaoglu, N. B., K. Demirkol, Y., Doganay, L., Ergul, Y., & Karacan, M., (2022). Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1. JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY , vol.33, no.2, 262-273.

AKGÜN DOĞAN, ÖZLEM Et Al. "Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1," JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY , vol.33, no.2, 262-273, 2022

AKGÜN DOĞAN, ÖZLEM A. Et Al. "Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1." JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY , vol.33, no.2, pp.262-273, 2022

AKGÜN DOĞAN, Ö. Et Al. (2022) . "Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1." JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY , vol.33, no.2, pp.262-273.

@article{article, author={ÖZLEM AKGÜN DOĞAN Et Al. }, title={Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1}, journal={JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY}, year=2022, pages={262-273} }