Salar, S. Et Al. 2012. Four novel and two recurrent NHLRC1 (EPM2B) and EPM2A gene mutations leading to Lafora disease in six Turkish families. EPILEPSY RESEARCH , vol.98 , 273-276.

Salar, S., Yeni, N., Gunduz, A., GÜLER, A., GÖKÇAY, A., VELİOĞLU, S., ... Gundogdu, A.(2012). Four novel and two recurrent NHLRC1 (EPM2B) and EPM2A gene mutations leading to Lafora disease in six Turkish families. EPILEPSY RESEARCH , vol.98, 273-276.

Salar, Seda Et Al. "Four novel and two recurrent NHLRC1 (EPM2B) and EPM2A gene mutations leading to Lafora disease in six Turkish families," EPILEPSY RESEARCH , vol.98, 273-276, 2012

Salar, Seda Et Al. "Four novel and two recurrent NHLRC1 (EPM2B) and EPM2A gene mutations leading to Lafora disease in six Turkish families." EPILEPSY RESEARCH , vol.98, pp.273-276, 2012

Salar, S. Et Al. (2012) . "Four novel and two recurrent NHLRC1 (EPM2B) and EPM2A gene mutations leading to Lafora disease in six Turkish families." EPILEPSY RESEARCH , vol.98, pp.273-276.

@article{article, author={Seda Salar Et Al. }, title={Four novel and two recurrent NHLRC1 (EPM2B) and EPM2A gene mutations leading to Lafora disease in six Turkish families}, journal={EPILEPSY RESEARCH}, year=2012, pages={273-276} }