The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis

✍ Scribed by Janneke M. Stapelbroek; Casper W. Bollen; Johannes K. Ploos van Amstel; Karel J. van Erpecum; Jan van Hattum; Leonard H. van den Berg; Leo W.J. Klomp; Roderick H.J. Houwen

• Book ID: 116650447
• Publisher: Elsevier Science
• Year: 2004
• Tongue: English
• Weight: 110 KB
• Volume: 41
• Category: Article
• ISSN: 0168-8278
• DOI: 10.1016/j.jhep.2004.07.017