A novel MAOA gene variant: Brunner syndrome, a rare syndrome, is associated with a wide range of psychiatric symptoms

Documenti analoghi

• Phenotypes of autism spectrum disorder and schizoaffective disorder associated with SETD1B gene but without intellectual disability and seizures
  di: Gül Ünsel‐Bolat, et al.
  Pubblicazione: (2024)
• Cohen syndrome: Can early‐onset recurrent infections and hypotonia provide early diagnosis and intervention for intellectual disability?
  di: Gül Ünsel‐Bolat, et al.
  Pubblicazione: (2024)
• Investigation of patients with childhood epilepsy in single center: Comprehensive genetic testing experience
  di: Hamide Betul Gerik‐Celebi, et al.
  Pubblicazione: (2024)
• Testing DAT1 and DRD4 Genes in Attention Deficit Hyperactivity Disorder Using a Wide Spectrum of Neurocognitive Batteries
  di: Gül Ünsel‐Bolat, et al.
  Pubblicazione: (2026)
• Could Transforming Growth Factor Beta and Target MicroRNA Dysregulation Serve as Biomarkers of Symptom Severity in Patients With Obsessive‐Compulsive Disorder?
  di: Sinan Altunoz, et al.
  Pubblicazione: (2025)