Mutations in SLC6A17 cause autosomal-recessive intellectual disability

Clin Genet. 2015 Aug;88(2):136-7. doi: 10.1111/cge.12610. Epub 2015 Jun 3.
No abstract available

Publication types

  • Comment

MeSH terms

  • Amino Acid Transport Systems / genetics*
  • Animals
  • Female
  • Homozygote*
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Mental Disorders / genetics*
  • Plasma Membrane Neurotransmitter Transport Proteins / genetics*
  • Speech Disorders / genetics*
  • Tremor / genetics*

Substances

  • Amino Acid Transport Systems
  • Plasma Membrane Neurotransmitter Transport Proteins