A novel mutation in HEXB that causing Infantil Sandhoff Disease


Akçakaya N. H., Özdemir Ö., Uğur İşeri S. A., Yücesan E., Özbek U., Yapıcı Z.

American Society of Human Genetics (ASHG), , Vancouver, Canada, 18 - 22 October 2016, pp.1

  • Publication Type: Conference Paper / Summary Text
  • City: Vancouver
  • Country: Canada
  • Page Numbers: pp.1
  • Bezmialem Vakıf University Affiliated: No