Genetic insights into the causes and classification of the cerebral palsies

This publication has 118 references indexed in Scilit:

• Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature
  The American Journal of Human Genetics, 2011
• Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
  Nature Genetics, 2011
• Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis
  Genome Research, 2011
• Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study
  The Lancet Neurology, 2011
• Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome
  Nature Genetics, 2010
• Sorting of the Alzheimer's Disease Amyloid Precursor Protein Mediated by the AP-4 Complex
  Developmental Cell, 2010
• Exome sequencing identifies the cause of a mendelian disorder
  Nature Genetics, 2009
• Mutation in the AP4M1 Gene Provides a Model for Neuroaxonal Injury in Cerebral Palsy
  The American Journal of Human Genetics, 2009
• The Genetic Basis of Complex Traits
  2007
• Adaptable adaptors for coated vesicles
  Trends in Cell Biology, 2004