## Abstract Wilson's disease (WD) is an autosomal recessive disorder characterized by the functional disruption of the copperβtransporting protein adenosine triphosphatase 7B (ATPβase 7B). The disease is caused by mutations in __ATP7B__ gene. It seems that the type of mutation in __ATP7B__ only to
β¦ LIBER β¦
Characteristics of monozygotic male and female twins discordant for overweight: A descriptive study
β Scribed by Karen S. Mitchell; Suzanne E. Mazzeo; Steven H. Aggen; Hermine H. Maes; Kenneth S. Kendler; Michael C. Neale; Cynthia M. Bulik
- Book ID
- 116415372
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 116 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1471-0153
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