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 Ö. M. , ...More

The European Human Genetics Conference, Barselona, Spain, 21 - 24 May 2016, pp.354

  • Publication Type: Conference Paper / Full Text
  • City: Barselona
  • Country: Spain
  • Page Numbers: pp.354