TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function

Παρόμοια τεκμήρια

• Spatial Clustering of de Novo Missense Mutations Identifies Candidate Neurodevelopmental Disorder-Associated Genes
  ανά: Lelieveld, Stefan H., κ.ά.
  Έκδοση: (2017)
• Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation
  ανά: Acuna-Hidalgo, Rocio, κ.ά.
  Έκδοση: (2015)
• Recurrent De Novo Mutations in PACS1 Cause Defective Cranial-Neural-Crest Migration and Define a Recognizable Intellectual-Disability Syndrome
  ανά: Schuurs-Hoeijmakers, Janneke H.M., κ.ά.
  Έκδοση: (2012)
• De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila
  ανά: Lugtenberg, Dorien, κ.ά.
  Έκδοση: (2016)
• Platform comparison of detecting copy number variants with microarrays and whole-exome sequencing
  ανά: de Ligt, Joep, κ.ά.
  Έκδοση: (2014)