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  • Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln

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Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln

Authors

  • Saara Finnilä aDepartment of Neurology, University of Oulu, PO Box 5000, FIN-90014 University of Oulu, Oulu, Finland, bDepartment of Medical Biochemistry, University of Oulu, Oulu, Finland, cBiocenter, University of Oulu, Oulu, Finland, dDepartment of Neurology, University of Kuopio, Kuopio, Finland, eDNA and Chromosome Laboratory, Kuopio University Hospital, Kuopio, Finland PubMed articlesGoogle scholar articles
  • Jaana Autere aDepartment of Neurology, University of Oulu, PO Box 5000, FIN-90014 University of Oulu, Oulu, Finland, bDepartment of Medical Biochemistry, University of Oulu, Oulu, Finland, cBiocenter, University of Oulu, Oulu, Finland, dDepartment of Neurology, University of Kuopio, Kuopio, Finland, eDNA and Chromosome Laboratory, Kuopio University Hospital, Kuopio, Finland PubMed articlesGoogle scholar articles
  • Maarit Lehtovirta aDepartment of Neurology, University of Oulu, PO Box 5000, FIN-90014 University of Oulu, Oulu, Finland, bDepartment of Medical Biochemistry, University of Oulu, Oulu, Finland, cBiocenter, University of Oulu, Oulu, Finland, dDepartment of Neurology, University of Kuopio, Kuopio, Finland, eDNA and Chromosome Laboratory, Kuopio University Hospital, Kuopio, Finland PubMed articlesGoogle scholar articles
  • Päivi Hartikainen aDepartment of Neurology, University of Oulu, PO Box 5000, FIN-90014 University of Oulu, Oulu, Finland, bDepartment of Medical Biochemistry, University of Oulu, Oulu, Finland, cBiocenter, University of Oulu, Oulu, Finland, dDepartment of Neurology, University of Kuopio, Kuopio, Finland, eDNA and Chromosome Laboratory, Kuopio University Hospital, Kuopio, Finland PubMed articlesGoogle scholar articles
  • Arto Mannermaa aDepartment of Neurology, University of Oulu, PO Box 5000, FIN-90014 University of Oulu, Oulu, Finland, bDepartment of Medical Biochemistry, University of Oulu, Oulu, Finland, cBiocenter, University of Oulu, Oulu, Finland, dDepartment of Neurology, University of Kuopio, Kuopio, Finland, eDNA and Chromosome Laboratory, Kuopio University Hospital, Kuopio, Finland PubMed articlesGoogle scholar articles
  • Hilkka Soininen aDepartment of Neurology, University of Oulu, PO Box 5000, FIN-90014 University of Oulu, Oulu, Finland, bDepartment of Medical Biochemistry, University of Oulu, Oulu, Finland, cBiocenter, University of Oulu, Oulu, Finland, dDepartment of Neurology, University of Kuopio, Kuopio, Finland, eDNA and Chromosome Laboratory, Kuopio University Hospital, Kuopio, Finland PubMed articlesGoogle scholar articles
  • Kari Majamaa aDepartment of Neurology, University of Oulu, PO Box 5000, FIN-90014 University of Oulu, Oulu, Finland, bDepartment of Medical Biochemistry, University of Oulu, Oulu, Finland, cBiocenter, University of Oulu, Oulu, Finland, dDepartment of Neurology, University of Kuopio, Kuopio, Finland, eDNA and Chromosome Laboratory, Kuopio University Hospital, Kuopio, Finland PubMed articlesGoogle scholar articles
  1. Dr Majamaa, kari.majamaa{at}oulu.fi
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Citation

Finnilä S, Autere J, Lehtovirta M, et al
Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln
Journal of Medical Genetics 2001;38:400-405.

Publication history

  • First published June 1, 2001.
Online issue publication 
March 15, 2021

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Journal of Medical Genetics