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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
Yuti Nakhwa, Dr
Su uso est destinado a complementar dietas insuficientes
In this article, we explore markers of oxidative stress, direct and indirect strategies to detect oxidative stress, cellular antioxidants that protect against oxidative stress
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