A First Turkish Case Report of a Colloidan Baby with a Postmortem Diagnosis of type II Gaucher Disease and a Novel Mutation Detected by Exom Sequencing.


ÖNENLİ MUNGAN H. N. , Ceylaner S., balcı s., KOR D. , Şeker-Yılmaz B.

13 th Annual World Symposium, 10 - 13 Şubat 2014

  • Yayın Türü: Bildiri / Özet Bildiri