P17.5 Familial Very long chain Acetyl CoA dehydrogenase deficiency (VLCAD) as a cause of neonatal sudden infant death: could survival in VLCAD deficiency be improved by prompt diagnosis?

✍ Scribed by E. Scalais; J. Bottu; C. Nuttin; C. Boulanger; R. Wanders; L. De Meirleir

• Book ID: 114360589
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 36 KB
• Volume: 15
• Category: Article
• ISSN: 1090-3798
• DOI: 10.1016/s1090-3798(11)70346-4