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uneia dintre companiile aparinnd grupului Vision Healthcare

B., Young, J

Extensive counseling is recommended when using certain agents

Mutations in CPT1 can cause carnitine palmitoyltransferase I (CPT I) deficiency, which is an autosomal recessive genetic condition (need two copies of the mutation)

Approximately 11% of children 4-17 years of age (6.4 million) have been diagnosed with ADHD as of 2011 (1)
