Source:http://linkedlifedata.com/resource/pubmed/id/17478391
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
2007-5-16
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
1167-1122
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
17
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
247-8
|
| pubmed:meshHeading |
pubmed-meshheading:17478391-Adult,
pubmed-meshheading:17478391-Asian Continental Ancestry Group,
pubmed-meshheading:17478391-China,
pubmed-meshheading:17478391-DNA Mutational Analysis,
pubmed-meshheading:17478391-Female,
pubmed-meshheading:17478391-Frameshift Mutation,
pubmed-meshheading:17478391-Humans,
pubmed-meshheading:17478391-Male,
pubmed-meshheading:17478391-Pedigree,
pubmed-meshheading:17478391-Pigmentation Disorders,
pubmed-meshheading:17478391-Skin
|
| pubmed:articleTitle |
Novel deletion mutation of DSRAD in a Chinese family with Dyschromatosis Symmetrica Hereditaria (DSH).
|
| pubmed:publicationType |
Letter
|