Wilson disease: a most unusual patient

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Bibliographic Details
Published inQJM : An International Journal of Medicine Vol. 109; no. 2; pp. 117 - 118
Main Author Walshe, J M
Format Journal Article
LanguageEnglish
Published England 01.02.2016
Subjects
Adenosine Triphosphatases - genetics
Asymptomatic Diseases - psychology
Cation Transport Proteins - genetics
Ceruloplasmin - analysis
Copper - analysis
Copper-transporting ATPases
Female
Hepatolenticular Degeneration - blood
Hepatolenticular Degeneration - diagnosis
Hepatolenticular Degeneration - genetics
Hepatolenticular Degeneration - physiopathology
Homozygote
Humans
Liver - pathology
Middle Aged
Mutation
Siblings
Treatment Refusal
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Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
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content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:1460-2725
1460-2393
DOI:10.1093/qjmed/hcv142