Wilson disease is an autosomal recessive disorder of copper transport resulting from the defective function of a copper transporting P-type ATPasi (ATP7B). We have carried out mutational analysis in 295 patients of Mediterranean origin with Wilson Disease, including 85 Sardinians, 120 Continental It
✦ LIBER ✦
Haplotype and mutation analysis in Greek patients with Wilson disease
✍ Scribed by Loudianos, Georgios; Dessì, Valeria; Lovicu, Mario; Angius, Andrea; Kanavakis, Emmanuel; Tzetis, Maria; Kattamis, Christos; Manolaki, Nina; Vassiliki, Getsi; Karpathios, Themistoklis
- Book ID
- 110024728
- Publisher
- Nature Publishing Group
- Year
- 1998
- Tongue
- English
- Weight
- 82 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1018-4813
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