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Journal of Medical Genetics logoLink to Journal of Medical Genetics
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. 2001 Jun;38(6):400–405. doi: 10.1136/jmg.38.6.400

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

S Finnila, J Autere, M Lehtovirta, P Hartikainen, A Mannermaa, H Soininen, K Majamaa
PMCID: PMC1734884  PMID: 11424923

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