New Horizons in Correction of Mutated ATP7B in Wilson Disease Using Pharmacological Agents: Precise Medicine
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Biochemistry
Link
http://link.springer.com/content/pdf/10.1007/s12291-019-00855-8.pdf
Reference12 articles.
1. Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW. The Wilson’s disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat Genet. 1993;5:327–37.
2. Thomas GR, Forbes JR, Walshe JM, Roberts EA, Cox DW. The Wilson disease gene spectrum of mutations and their consequences. Nat Genet. 1995;9:210–7.
3. Gitlin JD. Wilson disease. Gastroenterology. 2003;123:1868–77.
4. Gao J, Brackley S, Mann JP. The global prevalence of Wilson disease from next generation sequencing data. Genet Med. 2018. https://doi.org/10.1038/s41436-018-0309-9 .
5. Coffey AJ, Durkie M, Hague S, Mclay K, et al. A genetic study of Wilson disease in the United Kingdom. Brain. 2013;136:1476–87.
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