ZEB2 nokta mutasyonuna bağlı Mowat-Wilson sendromu
ORPHA:261552· ICD-10 Q43.1· Mowat-Wilson syndrome due to a ZEB2 point mutation
- Kalıtım
- Autosomal dominant
- Başlangıç yaşı
- Antenatal, Neonatal
ORPHA:261552· ICD-10 Q43.1· Mowat-Wilson syndrome due to a ZEB2 point mutation