Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy

Clin Genet. 2015 Dec;88(6):597-9. doi: 10.1111/cge.12581. Epub 2015 Mar 30.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Brain Diseases / genetics*
  • Child, Preschool
  • Codon, Nonsense*
  • Developmental Disabilities / genetics*
  • Exome / genetics
  • Genes, Recessive
  • Genetic Predisposition to Disease / genetics*
  • Genotype
  • Humans
  • Language Development Disorders / genetics
  • Magnetic Resonance Imaging
  • Male
  • Membrane Proteins / genetics*
  • Phosphoric Monoester Hydrolases / genetics*
  • Sequence Analysis, DNA

Substances

  • Codon, Nonsense
  • Membrane Proteins
  • PGAP1 protein, human
  • Phosphoric Monoester Hydrolases