Homozygous mutations in the conserved ATP hinge region of the Wilson disease gene: Association with liver disease Academic Article uri icon

Overview

MeSH Major

  • Adenosine Triphosphatases
  • Cation Transport Proteins
  • Hepatolenticular Degeneration
  • Homozygote
  • Liver Diseases
  • Mutation

abstract

  • We hereby report the association of liver disease with homozygous mutations in the conserved ATP hinge region of exon 18 of the ATP7B gene.

publication date

  • July 2010

Research

keywords

  • Academic Article

Identity

Language

  • eng

Digital Object Identifier (DOI)

  • 10.1097/MCG.0b013e3181ce5138

PubMed ID

  • 20485189

Additional Document Info

start page

  • 432

end page

  • 9

volume

  • 44

number

  • 6