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Article

Genetic and environmental modifiers of Wilson disease.

Handbook of clinical neurology - 1 Jan 2017

Medici Valentina, Weiss Karl-Heinz

Abstract excerpt

Wilson disease (WD) is characterized by remarkable variety in its phenotypic presentation. Patients with WD can present with hepatic, neurologic, and psychiatric symptoms combined in different and unpredictable ways. Importantly, no convincing phenotype-genotype correlation has ever been identified, opening the possibility that other genes, aside from ATPase copper-transporting beta (ATP7B), are involved in the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28433108
DOI: 10.1016/B978-0-444-63625-6.00004-5

Genes

APOE
ATOX1
COMMD1
HFE
MTHFR
XIAP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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