ŞAHİN, İ. Et Al. 2018. Becker's myotonia: novel mutations and clinical variability in patients born to consanguineous parents. ACTA NEUROLOGICA BELGICA , vol.118, no.4 , 567-572.

ŞAHİN, İ., ERDEM, H. B., TAN, H., & TATAR, A., (2018). Becker's myotonia: novel mutations and clinical variability in patients born to consanguineous parents. ACTA NEUROLOGICA BELGICA , vol.118, no.4, 567-572.

ŞAHİN, İbrahim Et Al. "Becker's myotonia: novel mutations and clinical variability in patients born to consanguineous parents," ACTA NEUROLOGICA BELGICA , vol.118, no.4, 567-572, 2018

ŞAHİN, İbrahim Et Al. "Becker's myotonia: novel mutations and clinical variability in patients born to consanguineous parents." ACTA NEUROLOGICA BELGICA , vol.118, no.4, pp.567-572, 2018

ŞAHİN, İ. Et Al. (2018) . "Becker's myotonia: novel mutations and clinical variability in patients born to consanguineous parents." ACTA NEUROLOGICA BELGICA , vol.118, no.4, pp.567-572.

@article{article, author={İbrahim ŞAHİN Et Al. }, title={Becker's myotonia: novel mutations and clinical variability in patients born to consanguineous parents}, journal={ACTA NEUROLOGICA BELGICA}, year=2018, pages={567-572} }