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We report on the performance of whole-exome sequencing in members of a consanguineous family with a history of pediatric hypertrophic cardiomyopathy and sudden cardiac death, which led to the identification of a homozygous stop variant in the SLC22A5 gene, implicated in primary carnitine deficiency, as the likely genetic cause

Among these genes, L3MBTL1 , TNIP1 , HAT1 , and BEND6 have also been shown to be correlated with low AF content [53]

While the formula does include artificial sweeteners and food dyes, it still checks the box for essential pre-workout support

international journal of clinical chemistry 2021