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