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
| Autor: | Tonin, Rodolfo, Caciotti, Anna, Funghini, Silvia, Pasquini, Elisabetta, Mooney, Sean D., Cai, Binghuang, Proncopio, Elena, Donati, Maria Alice, Baronio, Federico, Bettocchi, Ilaria, Cassio, Alessandra, Biasucci, Giacomo, Bordugo, Andrea, la Marca, Giancarlo, Guerrini, Renzo, Morrone, Amelia |
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| Zdroj: | In BBA Clinical June 2016 5:114-119 |
| Databáze: | ScienceDirect |
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