Sindromi miasteniche congenite con disturbo della glicosilazione
ORPHA:353327· ICD-10 G70.2· Congenital myasthenic syndrome with glycosylation defect
- Prevalenza
- Unknown
- Trasmissione
- Autosomal recessive
- Età di esordio
- Infancy, Neonatal
ORPHA:353327· ICD-10 G70.2· Congenital myasthenic syndrome with glycosylation defect