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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

Protein hingegen bietet langanhaltende Energie, die sowohl whrend des Trainings als auch danach die Energielevel des Krpers untersttzt

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

Values are presented as arithmetic mean SD for all participants ( n = 16)

Grivas, The Role of L-Carnitine in Distance Athletes, International Journal of Sports Science, Vol