Novel human pathological mutations. Gene symbol: TAP2. Disease: HLA class I deficiency

Hum Genet. 2007 Jun;121(5):646-7.
No abstract available

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 3
  • ATP-Binding Cassette Transporters / genetics*
  • HLA Antigens / immunology*
  • Humans
  • Immune System Diseases / genetics*
  • Mutation

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 3
  • ATP-Binding Cassette Transporters
  • HLA Antigens
  • TAP2 protein, human