[Hartnup disease is related to a mutation in the SL C6A19 gene coding for the B degrees AT1 aminoacid transporter]

Ann Dermatol Venereol. 2005 Aug-Sep;132(8-9 Pt 1):726. doi: 10.1016/s0151-9638(05)79430-8.
[Article in French]
No abstract available

Publication types

  • News

MeSH terms

  • Amino Acid Transport System A / genetics
  • Amino Acid Transport Systems, Neutral / genetics*
  • Hartnup Disease / genetics*
  • Humans
  • Mutation

Substances

  • Amino Acid Transport System A
  • Amino Acid Transport Systems, Neutral
  • SLC6A19 protein, human