Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression

  • A Vihola
  • , J Palmio
  • , O Danielsson
  • , S Penttilä
  • , D Louiselle
  • , S Pittman
  • , C Weihl
  • , B Udd

    Research output: Contribution to journalArticleScientificpeer-review

    23 Citations (Scopus)
    Original languageEnglish
    Article numbere337
    Pages (from-to)e337
    JournalNeurology: Genetics
    Volume5
    Issue number3
    DOIs
    Publication statusPublished - 2019
    Publication typeA1 Journal article-refereed

    Publication forum classification

    • Publication forum level 1

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