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Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.

Translated title of the contribution: Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.
  • R Kleta
  • , E. Romeo
  • , Z. Ristic
  • , T. Ohura
  • , C. Stuart
  • , M. Arcos-Burgos
  • , M.H. Dave
  • , C.A. Wagner
  • , S.R. Camargo
  • , S. Inoue
  • , N. Matsuura
  • , A. Helip-Wooley
  • , D. Bockenhauer
  • , R. Warth
  • , I. Bernardini
  • , G. Visser
  • , T. Eggerman
  • , P. Lee
  • , A. Chairoungdua
  • , P. Jutabha
  • E. Babu, S. Nilwarangkoon, N. Anzai, Y. Kanai, F. Verrey, W.A. Gahl, A. Koizumi

Research output: Contribution to journalArticleAcademicpeer-review

Translated title of the contributionMutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.
Original languageUndefined/Unknown
Pages (from-to)999-1002
Number of pages4
JournalNature Genetics
Volume36
Issue number9
Publication statusPublished - 2004

Keywords

  • Econometric and Statistical Methods: General
  • Genetics
  • Geneeskunde(GENK)
  • Algemeen onderzoek

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