SNX14 Sorting Nexin 14 gene mutation causes a new syndromic form of cerebellar atrophy in a Turkish family


ÖZGÜL R. K. , YÜCEL YILMAZ D. , Ömer g., YALNIZOĞLU D. , Mahmut s., DURSUN A.

SSIEM, 4 - 07 September 2015

  • Publication Type: Conference Paper