RAI1 Transcription Factor Activity Is Impaired in Mutants Associated with Smith-Magenis Syndrome

समान संसाधन

• Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome
  द्वारा: Carmona-Mora, Paulina, और अन्य
  प्रकाशित: (2010)
• Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith–Magenis syndrome
  द्वारा: Vieira, Gustavo H, और अन्य
  प्रकाशित: (2012)
• A Rare De Novo RAI1 Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation
  द्वारा: Abad, Clemer, और अन्य
  प्रकाशित: (2018)
• Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic Behavior
  द्वारा: Carmona-Mora, Paulina, और अन्य
  प्रकाशित: (2010)
• RAI1 gene mutations: mechanisms of Smith–Magenis syndrome
  द्वारा: Falco, Mariateresa, और अन्य
  प्रकाशित: (2017)