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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
10
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pubmed:dateCreated |
2010-9-13
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pubmed:abstractText |
Although many mutations of the Wilson's disease (WD) gene (ATP7B) have been reported, few data exist regarding the occurrence of fulminant hepatic failure (FHF). We sought to determine if genotypic assignment according to type of protein-product could be related to the prevalence of FHF among patients with WD.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1502-7708
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pubmed:author |
pubmed-author:AoyagiHiroyukiH,
pubmed-author:HasataniKenkeiK,
pubmed-author:HayashiHisaoH,
pubmed-author:HayashiYoshiakiY,
pubmed-author:KanekoYoshibumiY,
pubmed-author:MibayashiHiroshiH,
pubmed-author:MiwaKazuhiroK,
pubmed-author:OkadaToshihideT,
pubmed-author:ShionoYutaY,
pubmed-author:TsujiShigetsuguS,
pubmed-author:YamagishiMasakazuM,
pubmed-author:YoshimitsuMasashiM
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pubmed:issnType |
Electronic
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1232-7
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pubmed:meshHeading |
pubmed-meshheading:20491539-Adenosine Triphosphatases,
pubmed-meshheading:20491539-Adolescent,
pubmed-meshheading:20491539-Alleles,
pubmed-meshheading:20491539-Base Sequence,
pubmed-meshheading:20491539-Biological Markers,
pubmed-meshheading:20491539-Cation Transport Proteins,
pubmed-meshheading:20491539-Child,
pubmed-meshheading:20491539-Codon, Nonsense,
pubmed-meshheading:20491539-Female,
pubmed-meshheading:20491539-Genotype,
pubmed-meshheading:20491539-Hepatolenticular Degeneration,
pubmed-meshheading:20491539-Humans,
pubmed-meshheading:20491539-Japan,
pubmed-meshheading:20491539-Liver Failure, Acute,
pubmed-meshheading:20491539-Male,
pubmed-meshheading:20491539-Mutagenesis, Insertional,
pubmed-meshheading:20491539-Mutation,
pubmed-meshheading:20491539-Mutation, Missense,
pubmed-meshheading:20491539-Pedigree,
pubmed-meshheading:20491539-Phenotype,
pubmed-meshheading:20491539-Prevalence,
pubmed-meshheading:20491539-Sequence Deletion
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pubmed:year |
2010
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pubmed:articleTitle |
High prevalence of fulminant hepatic failure among patients with mutant alleles for truncation of ATP7B in Wilson's disease.
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pubmed:affiliation |
Department of Internal Medicine, Kanazawa University Graduate School of Medical Science, Ishikawa, Japan. okada351116@yahoo.co.jp
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pubmed:publicationType |
Journal Article,
Comparative Study
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