Source:http://linkedlifedata.com/resource/pubmed/id/21080147
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
2010-11-16
|
| pubmed:abstractText |
Atrioventricular septal defects (AVSDs) occur as clinical defects of several different syndromes, as autosomal dominant defects, and as sporadically occurring malformations. Consequently, there is genetic heterogeneity, but until recently, little is known about the genes involving in the pathogenesis of AVSD. CRELD1 gene, a novel cell adhesion molecule, is a candidate gene for AVSD.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Nov
|
| pubmed:issn |
1867-0687
|
| pubmed:author | |
| pubmed:issnType |
Electronic
|
| pubmed:volume |
6
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
348-52
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| pubmed:meshHeading |
pubmed-meshheading:21080147-Cell Adhesion Molecules,
pubmed-meshheading:21080147-Child,
pubmed-meshheading:21080147-Child, Preschool,
pubmed-meshheading:21080147-Extracellular Matrix Proteins,
pubmed-meshheading:21080147-Female,
pubmed-meshheading:21080147-Humans,
pubmed-meshheading:21080147-Infant,
pubmed-meshheading:21080147-Male,
pubmed-meshheading:21080147-Mitral Valve Insufficiency,
pubmed-meshheading:21080147-Mutation
|
| pubmed:year |
2010
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| pubmed:articleTitle |
Novel CRELD1 gene mutations in patients with atrioventricular septal defect.
|
| pubmed:affiliation |
Department of Cardiology, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China.
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| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|