Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference49 articles.
1. Al Jumah M, Majumdar R, Al Rajeh S, Awada A, Al Zaben A, Al Traif I et al (2004) clinical and genetic study of 56 Saudi Wilson disease patients: identification of Saudi-specific mutations. Eur J Neurol 11:121–124
2. Bachmann H, Lössner J, Kühn HJ, Siegemund R (1991) Occurrence, genetics and epidemiology of Wilson’s disease in east Germany. In: Czlonkowska A, van der Hamer CJA (eds) Proceedings of the 5th international symposium on Wilson's disease. Technical University Delft, pp 121–128
3. Caca K, Ferenci P, Kuhn HJ, Polli C, Willgerodt H, Kunath B et al (2001) High prevalence of the H1069Q mutation in East German patients with Wilson disease: rapid detection of mutations by limited sequencing and phenotype-genotype analysis. J Hepatol 35:575–581
4. Cater MA, Forbes J, La Fontaine S, Cox D, Mercer JFB (2004) Intracellular trafficking of the human Wilson protein: the role of the six N-terminal metal-binding sites. Biochem J 380:805–813
5. Curtis D, Durkie M, Balac P, Sheard D, Goodeve A. Peake I, Quarrell O, Tanner S. (1999) A study of Wilson disease mutations in Britain. Hum Mutat 14:304–311
Cited by
210 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献