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
  • Hacettepe University Affiliated: Yes