NMP029 Serial fetal and postnatal magnetic resonance imaging in a patient with Muscle Eye Brain disease with confirmed mutation in the POMGnT1 gene

✍ Scribed by A. Klein; E. Boltshauser; R. Mein; E. Clement; A. Solopova; T.A.G.M. Huisman

• Book ID: 114359741
• Publisher: Elsevier Science
• Year: 2007
• Tongue: English
• Weight: 44 KB
• Volume: 11
• Category: Article
• ISSN: 1090-3798
• DOI: 10.1016/s1090-3798(08)70687-1