A rare cause of intellectual disability: Novel mutation of ALKBH8 gene in two patients with intellectual developmental disorder, autosomal recessive type 71

YILMAZ UZMAN C., GÜRSOY S., AYYILDIZ EMECEN D., HAZAN F.

58th European Society of Human Genetics (ESHG) Conference, Milan, Italy, 24 - 27 May 2025, vol.33, pp.258-259, (Summary Text)

  • Publication Type: Conference Paper / Summary Text
  • Volume: 33
  • City: Milan
  • Country: Italy
  • Page Numbers: pp.258-259
  • Dokuz Eylül University Affiliated: Yes