Şahin, İ. Et Al. 2018. Becker’xxs myotonia: novel mutations and clinical variability in patients born to consanguineous parents.. Acta Neurologica Belgica .

Şahin, İ., Erdem, H. B., TAN, H., & TATAR, A., (2018). Becker’xxs myotonia: novel mutations and clinical variability in patients born to consanguineous parents.. Acta Neurologica Belgica .

Şahin, İbrahim Et Al. "Becker’xxs myotonia: novel mutations and clinical variability in patients born to consanguineous parents.," Acta Neurologica Belgica , 2018

Şahin, İbrahim Et Al. "Becker’xxs myotonia: novel mutations and clinical variability in patients born to consanguineous parents.." Acta Neurologica Belgica , 2018

Şahin, İ. Et Al. (2018) . "Becker’xxs myotonia: novel mutations and clinical variability in patients born to consanguineous parents.." Acta Neurologica Belgica .

@article{article, author={İbrahim ŞAHİN Et Al. }, title={Becker’xxs myotonia: novel mutations and clinical variability in patients born to consanguineous parents.}, journal={Acta Neurologica Belgica}, year=2018}