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PDFGenotype-phenotype correlations
Short report
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation
- Correspondence to Dr Ronen Spiegel, Department of Pediatrics B, Emek Medical Center, Afula 18101, Israel; spiegelr{at}zahav.net.il, spiegel_ro{at}clalit.org.il
Citation
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation
Publication history
- Received July 5, 2015
- Revised August 10, 2015
- Accepted August 11, 2015
- First published November 11, 2015.
Online issue publication
March 09, 2021
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- Data supplement 1 - Online figures
- Data supplement 2 - Online method
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