Intelligenzminderung, X-chromosomale, durch GRIA3-Mutationen
ORPHA:364028· ICD-10 F72· X-linked intellectual disability due to GRIA3 mutations
- Prävalenz
- <1 / 1 000 000
- Vererbung
- X-linked recessive
- Erkrankungsalter
- Infancy
ORPHA:364028· ICD-10 F72· X-linked intellectual disability due to GRIA3 mutations