Source:http://linkedlifedata.com/resource/pubmed/id/18482034
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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2008-5-16
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
1468-3083
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
22
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
750-1
|
pubmed:meshHeading |
pubmed-meshheading:18482034-Child,
pubmed-meshheading:18482034-Connexins,
pubmed-meshheading:18482034-Female,
pubmed-meshheading:18482034-Heterozygote,
pubmed-meshheading:18482034-Humans,
pubmed-meshheading:18482034-Malignant Atrophic Papulosis,
pubmed-meshheading:18482034-Mutation, Missense,
pubmed-meshheading:18482034-Polymerase Chain Reaction
|
pubmed:year |
2008
|
pubmed:articleTitle |
A new mutation in the GJB3 gene in a patient with erythrokeratodermia variabilis.
|
pubmed:publicationType |
Letter,
Case Reports
|