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A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated

  • T. Hornemann
  • , A. Penno
  • , S. Richard
  • , G. Nicholson
  • , F.S. van Dijk
  • , A. Rotthier
  • , V. Timmerman
  • , A. von Eckardstein

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)135-143
JournalNeurogenetics
Volume10
Issue number2
DOIs
Publication statusPublished - 2009

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