Skip to Main Content

Paper Details

Using whole-exome sequencing to identify inherited causes of autism.
Neuron
318
2013
AMT, ASD, ASDs, Mendelian disorders, PAH, PEX7, POMGNT1, SYNE1, VPS13B, autism, autism spectrum disorders, disease genes, genetic conditions, inherited risk alleles, patients
Author NameAffiliation
Timothy W YuBoston Children's Hospital
Timothy W YuBoston Children's Hospital
  • 1 - 2

Datasets

Release 1.2