Haryanyan, G. Et Al. 2021. The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey.. Journal of human genetics , vol.66, no.12 , 1145-1151.

Haryanyan, G., Ozdemir, O., Tutkavul, K., Dervent, A., Ayta, S., ÖZKARA, Ç., ... Salman, B.(2021). The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey.. Journal of human genetics , vol.66, no.12, 1145-1151.

Haryanyan, Garen Et Al. "The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey.," Journal of human genetics , vol.66, no.12, 1145-1151, 2021

Haryanyan, Garen Et Al. "The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey.." Journal of human genetics , vol.66, no.12, pp.1145-1151, 2021

Haryanyan, G. Et Al. (2021) . "The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey.." Journal of human genetics , vol.66, no.12, pp.1145-1151.

@article{article, author={Garen Haryanyan Et Al. }, title={The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey.}, journal={Journal of human genetics}, year=2021, pages={1145-1151} }