Peker, A. Et Al. 2022. Two novel mutations, two different clinical phenotypes associated with SCN5A; Brugada and Long QT syndromes. European Society of Human Genetics Conference 2022 , (Vienna, Austria), 1-2.

Peker, A., Toylu, A., Coşkun, M., Karamık, G., Altunbaş, F., Aracı, D. G., ... Öztürk, N.(2022). Two novel mutations, two different clinical phenotypes associated with SCN5A; Brugada and Long QT syndromes . European Society of Human Genetics Conference 2022 (pp.1-2). Vienna, Austria

Peker, ALP Et Al. "Two novel mutations, two different clinical phenotypes associated with SCN5A; Brugada and Long QT syndromes," European Society of Human Genetics Conference 2022, Vienna, Austria, 2022

Peker, ALP Et Al. "Two novel mutations, two different clinical phenotypes associated with SCN5A; Brugada and Long QT syndromes." European Society of Human Genetics Conference 2022 , Vienna, Austria, pp.1-2, 2022

Peker, A. Et Al. (2022) . "Two novel mutations, two different clinical phenotypes associated with SCN5A; Brugada and Long QT syndromes." European Society of Human Genetics Conference 2022 , Vienna, Austria, pp.1-2.

@conferencepaper{conferencepaper, author={ALP PEKER Et Al. }, title={Two novel mutations, two different clinical phenotypes associated with SCN5A; Brugada and Long QT syndromes}, congress name={European Society of Human Genetics Conference 2022}, city={Vienna}, country={Austria}, year={2022}, pages={1-2} }