A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2

✍ Scribed by Claudia Perandones; Federico E. Micheli; Luis A. Pellene; Marta A. Bayly; Samuel F. Berkovic; Leanne M. Dibbens

• Book ID: 112143466
• Publisher: John Wiley and Sons
• Year: 2012
• Tongue: English
• Weight: 192 KB
• Volume: 27
• Category: Article
• ISSN: 0885-3185
• DOI: 10.1002/mds.25083