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Description
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
For example, Yennurajalingam et al
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Raos, also not yet gone through the Campbells supply chain gauntlet rationalization bootcamp, still as savory as that night you went to the original restaurant in Harlem alongside all the sketchy goombas

Genetic variants influencing drug metabolism can facilitate the selection of pharmacological treatments, improving efficacy and reducing adverse effects

Periyasamy, S
