SMARCA5-related neurodevelopmental disorder is thought to be a rare condition with the exact prevalence currently unknown. All identified subjects have been autosomal dominant with most individuals harboring de novovariants.
SMARCA5SMARCA5SMARCA5-related neurodevelopmental disorder is thought to be a rare condition with the exact prevalence currently unknown. All identified subjects have been autosomal dominant with most individuals harboring de novovariants.