Source:http://linkedlifedata.com/resource/pubmed/id/20695004
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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2010-8-9
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pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
1531-8249
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
68
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
121-3
|
pubmed:meshHeading |
pubmed-meshheading:20695004-Genetic Predisposition to Disease,
pubmed-meshheading:20695004-Hereditary Central Nervous System Demyelinating Diseases,
pubmed-meshheading:20695004-Humans,
pubmed-meshheading:20695004-Mutation,
pubmed-meshheading:20695004-Myelin Sheath,
pubmed-meshheading:20695004-SOXE Transcription Factors
|
pubmed:year |
2010
|
pubmed:articleTitle |
Interruption of SOX10 function in myelinopathies.
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pubmed:publicationType |
Editorial,
Comment
|