Tonin, R., Caciotti, A., Funghini, S., Pasquini, E., Mooney, S. D., Cai, B., . . . Morrone, A. (2016). Clinical relevance of short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Exploring the role of new variants including the first SCAD-disease-causing allele carrying a synonymous mutation. BBA Clin.
Citação norma ChicagoTonin, Rodolfo, et al. "Clinical Relevance of Short-chain Acyl-CoA Dehydrogenase (SCAD) Deficiency: Exploring the Role of New Variants Including the First SCAD-disease-causing Allele Carrying a Synonymous Mutation." BBA Clin 2016.
Citação norma MLATonin, Rodolfo, et al. "Clinical Relevance of Short-chain Acyl-CoA Dehydrogenase (SCAD) Deficiency: Exploring the Role of New Variants Including the First SCAD-disease-causing Allele Carrying a Synonymous Mutation." BBA Clin 2016.