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Efectividad clínica del cribado neonatal de errores congénitos del metabolismo mediante espectrometría de masas en tándem. Parte III deficiencia primaria de carnitina (CUD), deficiencia de Acil-CoA deshidrogenasa de cadena corta (SCADD), deficiencia de Acil-CoA deshidrogenasa de cadena muy larga (VLCADD)96

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