P04.056- Anovel homozygous IFT122 p.I460N (c.1379T>A) mutation in Sensenbrenner syndrome: a rare disorder within two cousins.


AKALIN İ. , Elçioğlu N., Görmez Z., CANDAN C. , YILMAZ S. N. , Yücetürk B., ...More

European Conference of Human Genetics 2016, Barcelona, Spain, 21 May 2016, vol.24, no.1, pp.106

  • Publication Type: Conference Paper / Full Text
  • Volume: 24
  • City: Barcelona
  • Country: Spain
  • Page Numbers: pp.106