ERGÜN, U. Et Al. 2022. Genome-Wide Association and Whole Exome Sequencing Studies reveal a Novel Candidate Locus for Restless Legs Syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1 , 297-298.

ERGÜN, U., Say, B., Ergun, S. G., PERÇİN, F. E., Inan, L., Kaygisiz, S., ... Asal, P. G.(2022). Genome-Wide Association and Whole Exome Sequencing Studies reveal a Novel Candidate Locus for Restless Legs Syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 297-298.

ERGÜN, UFUK Et Al. "Genome-Wide Association and Whole Exome Sequencing Studies reveal a Novel Candidate Locus for Restless Legs Syndrome," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 297-298, 2022

ERGÜN, UFUK Et Al. "Genome-Wide Association and Whole Exome Sequencing Studies reveal a Novel Candidate Locus for Restless Legs Syndrome." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.297-298, 2022

ERGÜN, U. Et Al. (2022) . "Genome-Wide Association and Whole Exome Sequencing Studies reveal a Novel Candidate Locus for Restless Legs Syndrome." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.297-298.

@article{article, author={UFUK ERGÜN Et Al. }, title={Genome-Wide Association and Whole Exome Sequencing Studies reveal a Novel Candidate Locus for Restless Legs Syndrome}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2022, pages={297-298} }