Diagnosis for Wilson disease: this disease may not be a rare disease

J Gastroenterol. 2021 Jan;56(1):114-115. doi: 10.1007/s00535-020-01752-1. Epub 2021 Jan 3.

Author

Masaru Harada¹

Affiliation

¹ Third Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu, 807-8555, Japan. msrharada@med.uoeh-u.ac.jp.

PMID: 33392748
DOI: 10.1007/s00535-020-01752-1

No abstract available

Keywords: ATP7B; Ceruloplasmin; Genetic disease; Wilson disease.

Publication types

Editorial
Comment

MeSH terms

Adenosine Triphosphatases / genetics
Hepatolenticular Degeneration* / diagnosis
Hepatolenticular Degeneration* / genetics
Humans
Mutation
Rare Diseases / diagnosis

Substances

Adenosine Triphosphatases