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Paper Details

Case Report: Whole Exome Sequencing Identifies Compound Heterozygous Variants in <i>TSFM</i> Gene Causing Juvenile Hypertrophic Cardiomyopathy.
Front Cardiovasc Med
2
2022
Arg333Trp, Juvenile Hypertrophic Cardiomyopathy, Val119Leu, complex IV, hypertrophic cardiomyopathy, juvenile hypertrophic cardiomyopathy, lactic acidosis, mitochondrial hyperplasia, mitochondrial translation elongation factor, nuclear gene
Author NameAffiliation
Gary SatouDavid Geffen School of Medicine, University of California los angeles
Stanley F NelsonDavid Geffen School of Medicine, University of California los angeles
Stanley F NelsonDavid Geffen School of Medicine, University of California los angeles
Stanley F NelsonDavid Geffen School of Medicine, University of California los angeles
Stanley F NelsonInstitute for Precision Health, David Geffen School of Medicine, University of California los angeles
Stanley F NelsonDavid Geffen School of Medicine, University of California los angeles
Stanley F NelsonDavid Geffen School of Medicine, University of California los angeles
Stanley F NelsonDavid Geffen School of Medicine, University of California los angeles
Stanley F NelsonInstitute for Precision Health, David Geffen School of Medicine, University of California los angeles
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Release 1.2