A novel splicing site mutation of PLK4 that is required for centriole biogenesis and genomic stability causes Seckel syndrome

DİNÇER T., BUDAK G., SEMERCİ C. N., ÖLMEZ A., DODURGA Y., ÖZMERT M., ...Daha Fazla

European Society of Human Genetics Conference, 21 - 24 Mayıs 2016

  • Yayın Türü: Bildiri
  • Hacettepe Üniversitesi Adresli: Evet