Author:
Yuan Zhe-Feng,Wu Wei,Yu Yong-Lin,Shen Jue,Mao Shan-Shan,Gao Feng,Xia Zhe-Zhi
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Reference23 articles.
1. Geng J, Wang J, Yao RE, Liu XQ, Fu QH. Identification of one novel and nine recurrent mutations of the ATP7B gene in 11 children with Wilson disease. World J Pediatr 2013;9:158–162.
2. Coffey AJ, Durkie M, Hague S, McLay K, Emmerson J, Lo C, et al. A genetic study of Wilson’s disease in the United Kingdom. Brain 2013;136:1476–1487.
3. Aggarwal A, Bhatt M. Update on Wilson disease. Int Rev Neurobiol 2013;110:313–348.
4. Li XH, Lu Y, Ling Y, Fu QC, Xu J, Zang GQ, et al. Clinical and molecular characterization of Wilson’s disease in China: identification of 14 novel mutations. BMC Med Genet 2011;12: 6.
5. Squitti R, Polimanti R, Siotto M, Bucossi S, Ventriglia M, Mariani S, et al. ATP7B variants as modulators of copper dyshomeostasis in Alzheimer’s disease. Neuromolecular Med 2013;15:515–522.
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