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16879215
Source:
http://linkedlifedata.com/resource/pubmed/id/16879215
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0021201
,
umls-concept:C0026882
,
umls-concept:C0030705
,
umls-concept:C0040015
,
umls-concept:C0205314
,
umls-concept:C0205396
,
umls-concept:C0445356
,
umls-concept:C0679622
,
umls-concept:C1710133
,
umls-concept:C1880371
pubmed:issue
8
pubmed:dateCreated
2006-8-1
pubmed:abstractText
Glanzmann thrombasthenia (GT) is a congenital bleeding disorder caused by either a lack or dysfunction of the platelet integrin alphaIIbbeta3.
pubmed:grant
http://linkedlifedata.com/resource/pubmed/grant/M01-RR00102
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/101170508
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Fibrinogen
,
http://linkedlifedata.com/resource/pubmed/chemical/Platelet Glycoprotein GPIIb-IIIa...
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1538-7933
pubmed:author
pubmed-author:ChandyMM
,
pubmed-author:CollerB SBS
,
pubmed-author:NaikS LSL
,
pubmed-author:NelsonE J REJ
,
pubmed-author:PeretzHH
,
pubmed-author:SeligsohnUU
,
pubmed-author:SrivastavaAA
pubmed:issnType
Print
pubmed:volume
4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1730-7
pubmed:dateRevised
2007-12-3
pubmed:meshHeading
pubmed-meshheading:16879215-Adolescent
,
pubmed-meshheading:16879215-Adult
,
pubmed-meshheading:16879215-Binding Sites
,
pubmed-meshheading:16879215-Blood Platelets
,
pubmed-meshheading:16879215-Cell Membrane
,
pubmed-meshheading:16879215-Child
,
pubmed-meshheading:16879215-DNA Mutational Analysis
,
pubmed-meshheading:16879215-Female
,
pubmed-meshheading:16879215-Fibrinogen
,
pubmed-meshheading:16879215-Humans
,
pubmed-meshheading:16879215-Male
,
pubmed-meshheading:16879215-Mutation
,
pubmed-meshheading:16879215-Platelet Glycoprotein GPIIb-IIIa Complex
,
pubmed-meshheading:16879215-Polymorphism, Genetic
,
pubmed-meshheading:16879215-Polymorphism, Restriction Fragment Length
,
pubmed-meshheading:16879215-Thrombasthenia
pubmed:year
2006
pubmed:articleTitle
Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patients.
pubmed:affiliation
Department of Hematology, Christtian Medical College, Vellore, India.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't
,
Research Support, N.I.H., Extramural