The genetic landscape of childhood-onset dystonia in a nationwide Turkish cohort: Clinical spectrum, molecular diagnostics, and therapeutic implications

This publication has 45 references indexed in Scilit:

• Genetic Landscape of Dystonia in Asian Indians
  Movement Disorders Clinical Practice, 2025
• Chromosome Microarray Analysis for the Investigation of Deletions in Pediatric Movement Disorders: A Systematic Review of the Literature
  Movement Disorders Clinical Practice, 2023
• The Genetic Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders
  Movement Disorders, 2022
• The Prevalence of Idiopathic or Inherited Isolated Dystonia: A Systematic Review and Meta‐Analysis
  Movement Disorders Clinical Practice, 2022
• Genotype–Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review
  Movement Disorders, 2021
• Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single‐center cohort study
  Movement Disorders, 2019
• Genetic mimics of cerebral palsy
  Movement Disorders, 2019
• Excellent response to deep brain stimulation in a young girl with GNAO1-related progressive choreoathetosis
  Child's Nervous System, 2016
• The prevalence of primary dystonia: A systematic review and meta‐analysis
  Movement Disorders, 2012
• PRRT2 Mutations are the major cause of benign familial infantile seizures
  Human Mutation, 2012