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US$ 22.18
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Description
PMID: 30069296 7 A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features
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(36) found no significant liver enzyme improvement in pediatric patients, primarily based on a single pediatric study that itself showed no clear benefit (68)
Crmio 40 g (100% VRN*)
Le diagnostic en est fait par chographie ou scanner
