A mitochondrial tRNA val gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes

IFM Coo, EA Sistermans, IJ de Wijs, Coriene Catsman - Berrevoets, HFM (Herman) Busch, Jasper Scholte, Hans Klerk, BA van Oost, HJM Smeets

Research output: Contribution to journalArticleAcademicpeer-review

31 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)293-295
Number of pages3
Publication statusPublished - 1998

Research programs

  • EMC 05-04-21-02-00
  • EMC MM-01-54-01
  • EMC MM-04-44-02

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