A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease

✍ Scribed by Ramanath Majumdar; Mohammed Al Jumah; Saad Al Rajeh; Murray Fraser; Abdullah Al Zaben; Adnan Awada; Ibrahim Al Traif; Malcolm Paterson

• Book ID: 119465215
• Publisher: Elsevier Science
• Year: 2000
• Tongue: English
• Weight: 287 KB
• Volume: 179
• Category: Article
• ISSN: 0022-510X
• DOI: 10.1016/s0022-510x(00)00399-3