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Marked discordance for myopia in female monozygotic twins

✍ Scribed by Mohamed Dirani; Matthew Chamberlain; Pam Garoufalis; Christine Chen; Robyn H Guymer; Paul N Baird

Book ID
115180042
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
57 KB
Volume
34
Category
Article
ISSN
1442-6404

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## Abstract Wilson's disease (WD) is an autosomal recessive disorder characterized by the functional disruption of the copper‐transporting protein adenosine triphosphatase 7B (ATP‐ase 7B). The disease is caused by mutations in __ATP7B__ gene. It seems that the type of mutation in __ATP7B__ only to