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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
|
pubmed:dateCreated |
1997-12-18
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0340-5354
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
244
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
591-2
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9352458-Adolescent,
pubmed-meshheading:9352458-Adult,
pubmed-meshheading:9352458-Amino Acid Substitution,
pubmed-meshheading:9352458-Hepatolenticular Degeneration,
pubmed-meshheading:9352458-Histidine,
pubmed-meshheading:9352458-Humans,
pubmed-meshheading:9352458-Point Mutation,
pubmed-meshheading:9352458-Poland
|
pubmed:year |
1997
|
pubmed:articleTitle |
Very high frequency of the His1069Gln mutation in Polish Wilson disease patients.
|
pubmed:publicationType |
Letter,
Research Support, Non-U.S. Gov't
|