๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The Wilson disease gene: spectrum of mutations and their consequences

โœ Scribed by Thomas, Gordon R.; Forbes, John R.; Roberts, Eve A.; Walshe, John M.; Cox, Diane W.


Book ID
109915177
Publisher
Nature Publishing Group
Year
1995
Tongue
English
Weight
814 KB
Volume
9
Category
Article
ISSN
1061-4036

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Spectrum of Mutations in the Batten Dise
โœ Patricia B. Munroe; Hannah M. Mitchison; Angela M. O'Rawe; John W. Anderson; Ros ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› American Society of Human Genetics ๐ŸŒ English โš– 115 KB
Identification of novel ATP7B gene mutat
โœ Sangwook Park; Jung-Young Park; Gu-Hwan Kim; Jin-Ho Choi; Kyung-Mo Kim; Jong-Bae ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 281 KB ๐Ÿ‘ 1 views

## Communicated by Jurgen Horst Wilson disease (WND), an autosomal recessive disorder of copper transport, is characterized by excessive accumulation of intracellular copper in liver and extrahepatic tissues because of impaired biliary copper excretion and disturbed incorporation of copper into ce