A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease
Ramanath Majumdar, Mohammed Al Jumah, Saad Al Rajeh, Murray Fraser, Abdullah Al Zaben, Adnan Awada, Ibrahim Al Traif, Malcolm PatersonVolume:
179
Year:
2000
Language:
english
DOI:
10.1016/s0022-510x(00)00399-3
File:
PDF, 287 KB
english, 2000