Combined isobutyryl-CoA and multiple acyl-CoA dehydrogenase deficiency in a boy with altered riboflavin homeostasis.

Tummolo, Albina; Leone, Piero; Tolomeo, Maria; Solito, Rita; Mattiuzzo, Matteo; Lepri, Francesca Romana; Lorè, Tania; Cardinali, Roberta; De Giovanni, Donatella; Simonetti, Simonetta; Barile, Maria.

Afiliación

Tummolo A; Metabolic Diseases and Clinical Genetics Unit Children's Hospital "Giovanni XXIII" Bari Italy.
Leone P; Department of Biosciences, Biotechnology and Biopharmaceutics University of Bari "A. Moro" Bari Italy.
Tolomeo M; Department of Biosciences, Biotechnology and Biopharmaceutics University of Bari "A. Moro" Bari Italy.
Solito R; Department of Biosciences, Biotechnology and Biopharmaceutics University of Bari "A. Moro" Bari Italy.
Mattiuzzo M; Laboratory of Medical Genetics Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital Rome Italy.
Lepri FR; Laboratory of Medical Genetics Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital Rome Italy.
Lorè T; Regional Centre for Neonatal Screening Children's Hospital "Giovanni XXIII" Bari Italy.
Cardinali R; Regional Centre for Neonatal Screening Children's Hospital "Giovanni XXIII" Bari Italy.
De Giovanni D; Metabolic Diseases and Clinical Genetics Unit Children's Hospital "Giovanni XXIII" Bari Italy.
Simonetti S; Regional Centre for Neonatal Screening Children's Hospital "Giovanni XXIII" Bari Italy.
Barile M; Department of Biosciences, Biotechnology and Biopharmaceutics University of Bari "A. Moro" Bari Italy.