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Carnitine/Acylcarnitine Translocase Deficiency (Neonatal Phenotype): Successful Prenatal and Postmortem Diagnosis Associated with a Novel Mutation in a Single Family

Developmental AnomalyNeonatal PhenotypeNeonatologyInherited Metabolic DiseasePediatricsNewborn MedicinePrenatal DiagnosisCarnitine/acylcarnitine Translocase DeficiencyFetal ComplicationMedicineSingle Family