Diagnostic challenges in a severely delayed infant with hypersomnolence, failure to thrive and arteriopathy: A unique case of γ-hydroxybutyric aciduria and Williams syndrome

✍ Scribed by Ina Knerr; K. Michael Gibson; Jaya Ganesh; Michael J. Bennett; Gajja S. Salomons; Cornelis Jakobs; Scott M. Myers

• Publisher: John Wiley and Sons
• Year: 2007
• Tongue: English
• Weight: 52 KB
• Volume: 144B
• Category: Article
• ISSN: 1552-4841
• DOI: 10.1002/ajmg.b.30553