Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations

• Main Authors: De-Min Yu (Author), Zhou Feng (Author), Zang Guo-Qing (Author), Xu Jie (Author), Fu Qing-Chun (Author), Ling Yun (Author), Lu Yi (Author), Li Xin-Hua (Author), Han Yue (Author), Zhang Dong-Hua (Author), Gong Qi-Ming (Author), Lu Zhi-Meng (Author), Kong Xiao-Fei (Author), Wang Jian-She (Author), Zhang Xin-Xin (Author)
• Format: Book
• Published: BMC, 2011-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Wilson's disease (WND) is a rare autosomal recessive disorder. Here we have evaluated 62 WND cases (58 probands) from the Chinese Han population to expand our knowledge of <it>ATP7B </it>mutations and to more complet...