ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy.
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Am J Hum Genet. 2013 Aug 8;93(2):211-23. doi: 10.1016/j.ajhg.2013.06.006. Epub 2013 Jul 11.
Am J Hum Genet. 2013.
PMID: 23849775
Free PMC article.