Location and type of mutation in the LIS1 gene do not predict phenotypic severity

  • G Uyanik
  • , DJ Morris-Rosendahl
  • , J Stiegler
  • , J Klapecki
  • , C Gross
  • , Y Berman
  • , P Martin
  • , L Dey
  • , S Spranger
  • , GC Korenke
  • , I Schreyer
  • , C Hertzberg
  • , TE Neumann
  • , P Burkart
  • , C Spaich
  • , N Meng
  • , H Holthausen
  • , L Ades
  • , J Seidel
  • , E Mangold
  • G Buyse, P Meinecke, U Schara, C Zeschnigk, D Muller, G Helland, B Schulze, ML Wright, S Kortge-Jung, A Hehr, U Bogdahn, G Schuierer, J Kohlhase, Ludwig Aigner, G Wolff, U Hehr, J Winkler

    Research output: Contribution to journalOriginal Articlepeer-review

    32 Citations (Web of Science)
    Original languageEnglish
    Pages (from-to)442-447
    JournalNEUROLOGY
    Volume69
    Issue number5
    DOIs
    Publication statusPublished - 2007

    Keywords

    • SUBCORTICAL BAND HETEROTOPIA
    • ISOLATED LISSENCEPHALY SEQUENCE
    • MISSENSE MUTATIONS
    • DIEKER-SYNDROME
    • ACETYLHYDROLASE
    • MALFORMATION
    • MIGRATION
    • MALES

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