Novel variant related to SATB2‐associated syndrome

Documenti analoghi

• A novel MAOA gene variant: Brunner syndrome, a rare syndrome, is associated with a wide range of psychiatric symptoms
  di: Gül Ünsel‐Bolat, et al.
  Pubblicazione: (2024)
• The c.529G>A (p.Ala177Thr) RNASEH2B Gene Pathogenic Variant as a First‐Line Genetic Test for Aicardi‐Goutières Syndrome: A Case Series of Four Moroccan Families
  di: Mouna Ouhenach, et al.
  Pubblicazione: (2025)
• Melatonin attenuates affective disorders and cognitive deficits induced by perinatal exposure to a glyphosate‐based herbicide via antioxidant pathway in adult male and female rats
  di: Abdelghafour El Hamzaoui, et al.
  Pubblicazione: (2024)
• BDNF, proBDNF and proBDNF/BDNF ratio with electroencephalographic abnormalities in children with attention deficit hyperactivity disorder: Possible relations to cognition and severity
  di: Mostafa M. El‐Saied, et al.
  Pubblicazione: (2024)
• Compound heterozygous mutations in three Chinese patients of Segawa syndrome and their treatment outcomes
  di: Jie Zhang, et al.
  Pubblicazione: (2024)