Büyükgöl, F. Et Al. 2025. Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.. Scientific reports , vol.15, no.1 , 11682.

Büyükgöl, F., Gürdamar, B., Aluçlu, M. U., Beckmann, Y., Bilguvar, K., Boz, C., ... Bülbül, A.(2025). Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.. Scientific reports , vol.15, no.1, 11682.

Büyükgöl, Furkan Et Al. "Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.," Scientific reports , vol.15, no.1, 11682, 2025

Büyükgöl, Furkan Et Al. "Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.." Scientific reports , vol.15, no.1, pp.11682, 2025

Büyükgöl, F. Et Al. (2025) . "Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.." Scientific reports , vol.15, no.1, p.11682.

@article{article, author={Furkan Büyükgöl Et Al. }, title={Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.}, journal={Scientific reports}, year=2025, pages={11682} }