Copyright
©The Author(s) 2015.
World J Gastroenterol. Aug 7, 2015; 21(29): 8981-8984
Published online Aug 7, 2015. doi: 10.3748/wjg.v21.i29.8981
Published online Aug 7, 2015. doi: 10.3748/wjg.v21.i29.8981
Figure 1 ATP7B gene sequencing detected two heterozygous mutations (p.
A874V and p.N1270S) that have been reported to cause Wilson disease in the Wilson Disease Mutation Database (http://www.wilsondisease.med.ualberta.ca/database.asp), and predicted to be disease causing by Mutation Taster (http://www.mutationtaster.org).
- Citation: Abuduxikuer K, Li LT, Qiu YL, Wang NL, Wang JS. Wilson disease with hepatic presentation in an eight-month-old boy. World J Gastroenterol 2015; 21(29): 8981-8984
- URL: https://www.wjgnet.com/1007-9327/full/v21/i29/8981.htm
- DOI: https://dx.doi.org/10.3748/wjg.v21.i29.8981