ÖZGÜL, R. K. Et Al. 2015. SNX14 Sorting Nexin 14 gene mutation causes a new syndromic form of cerebellar atrophy in a Turkish family. SSIEM .

ÖZGÜL, R. K., YÜCEL YILMAZ, D., Ömer, g., YALNIZOĞLU, D., Mahmut, s., & DURSUN, A., (2015). SNX14 Sorting Nexin 14 gene mutation causes a new syndromic form of cerebellar atrophy in a Turkish family . SSIEM

ÖZGÜL, RIZA Et Al. "SNX14 Sorting Nexin 14 gene mutation causes a new syndromic form of cerebellar atrophy in a Turkish family," SSIEM, 2015

ÖZGÜL, RIZA K. Et Al. "SNX14 Sorting Nexin 14 gene mutation causes a new syndromic form of cerebellar atrophy in a Turkish family." SSIEM , 2015

ÖZGÜL, R. K. Et Al. (2015) . "SNX14 Sorting Nexin 14 gene mutation causes a new syndromic form of cerebellar atrophy in a Turkish family." SSIEM .

@conferencepaper{conferencepaper, author={RIZA KÖKSAL ÖZGÜL Et Al. }, title={SNX14 Sorting Nexin 14 gene mutation causes a new syndromic form of cerebellar atrophy in a Turkish family}, congress name={SSIEM}, city={}, country={}, year={2015}}