Molecular analysis and diagnosis in Japanese patients with Wilson's disease.
- 1 August 1999
- journal article
- research article
- Published by Wiley in Pediatrics International
- Vol. 41 (4) , 409-413
- https://doi.org/10.1046/j.1442-200x.1999.01092.x
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
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- High frequency of two mutations in codon 778 in exon 8 of the ATP7B gene in Taiwanese families with Wilson disease.Journal of Medical Genetics, 1996
- A Novel RNA Splicing Mutation in Japanese Patients with Wilson DiseaseBiochemical and Biophysical Research Communications, 1995
- The Wilson disease gene: spectrum of mutations and their consequencesNature Genetics, 1995
- The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease geneNature Genetics, 1993
- Mapping, cloning and genetic characterization of the region containing the Wilson disease geneNature Genetics, 1993
- The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes geneNature Genetics, 1993
- Isolation and Characterization of a Human Liver cDNA as a Candidate Gene for Wilson DiseaseBiochemical and Biophysical Research Communications, 1993