Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln
Open Access
- 1 June 2001
- journal article
- letter
- Published by BMJ in Journal of Medical Genetics
- Vol. 38 (6) , 400-405
- https://doi.org/10.1136/jmg.38.6.400
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
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