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When GHRH was administered to adolescents, their peak response was over 10 times greater than that seen in adults
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While not everyone received help, there are positive accounts of support teams offering refunds or replacements quickly
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
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