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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2011-6-7
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pubmed:abstractText |
Wide phenotypic and genotypic heterogeneities in Wilson's disease (WD) have been reported, hampering the study of their correlations. The goal of this study was to identify the factors related to these diversities.
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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 |
Jul
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pubmed:issn |
1478-3231
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pubmed:author |
pubmed-author:ChoiJin-HoJH,
pubmed-author:JinHye YHY,
pubmed-author:KimGu-HwanGH,
pubmed-author:KimJoo HJH,
pubmed-author:KimKwi-JooKJ,
pubmed-author:KimKyung MKM,
pubmed-author:LeeBeom HBH,
pubmed-author:LeeJin-JooJJ,
pubmed-author:LeeSun YSY,
pubmed-author:ParkJung-YoungJY,
pubmed-author:YooHan-WookHW
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pubmed:copyrightInfo |
© 2011 John Wiley & Sons A/S.
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pubmed:issnType |
Electronic
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
831-9
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pubmed:meshHeading |
pubmed-meshheading:21645214-Adenosine Triphosphatases,
pubmed-meshheading:21645214-Adolescent,
pubmed-meshheading:21645214-Adult,
pubmed-meshheading:21645214-Analysis of Variance,
pubmed-meshheading:21645214-Cation Transport Proteins,
pubmed-meshheading:21645214-Child,
pubmed-meshheading:21645214-Child, Preschool,
pubmed-meshheading:21645214-Codon, Nonsense,
pubmed-meshheading:21645214-DNA Mutational Analysis,
pubmed-meshheading:21645214-Frameshift Mutation,
pubmed-meshheading:21645214-Gene Frequency,
pubmed-meshheading:21645214-Genetic Association Studies,
pubmed-meshheading:21645214-Genetic Predisposition to Disease,
pubmed-meshheading:21645214-Hepatolenticular Degeneration,
pubmed-meshheading:21645214-Humans,
pubmed-meshheading:21645214-Infant,
pubmed-meshheading:21645214-Liver Diseases,
pubmed-meshheading:21645214-Middle Aged,
pubmed-meshheading:21645214-Mutation,
pubmed-meshheading:21645214-Mutation, Missense,
pubmed-meshheading:21645214-Nervous System Diseases,
pubmed-meshheading:21645214-Pedigree,
pubmed-meshheading:21645214-Phenotype,
pubmed-meshheading:21645214-Republic of Korea,
pubmed-meshheading:21645214-Time Factors,
pubmed-meshheading:21645214-Treatment Outcome,
pubmed-meshheading:21645214-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
Distinct clinical courses according to presenting phenotypes and their correlations to ATP7B mutations in a large Wilson's disease cohort.
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pubmed:affiliation |
Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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