Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene

  • S. Verhoef*
  • , R. Vrtel
  • , L. Bakker
  • , I. Stolte-Dijkstra
  • , M. Nellist
  • , J. H. Begeer
  • , J. Zaremba
  • , S. Jozwiak
  • , A. M.P. Tempelaars
  • , D. Lindhout
  • , D. J.J. Halley
  • , A. M.W. van den Ouweland
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)S85-S87
JournalHuman mutation
Volume11
Issue numberSUPPL 1
DOIs
Publication statusPublished - 1998
Externally publishedYes

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