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Whole genome and exome sequencing of monozygotic twins discordant for Crohn’s disease

✍ Scribed by Britt-Sabina Petersen,Martina E Spehlmann,Andreas Raedler,Björn Stade…


Book ID
126370238
Publisher
BioMed Central
Year
2014
Tongue
English
Weight
659 KB
Volume
15
Category
Article
ISSN
1471-2164

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## Abstract Wilson's disease (WD) is an autosomal recessive disorder characterized by the functional disruption of the copper‐transporting protein adenosine triphosphatase 7B (ATP‐ase 7B). The disease is caused by mutations in __ATP7B__ gene. It seems that the type of mutation in __ATP7B__ only to