Mowat-Wilson-Syndrom durch Punktmutationen im ZEB2-Gen
ORPHA:261552· ICD-10 Q43.1· Mowat-Wilson syndrome due to a ZEB2 point mutation
- Vererbung
- Autosomal dominant
- Erkrankungsalter
- Antenatal, Neonatal
ORPHA:261552· ICD-10 Q43.1· Mowat-Wilson syndrome due to a ZEB2 point mutation