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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1-2
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pubmed:dateCreated |
2009-4-27
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pubmed:abstractText |
Glanzmann's thrombasthenia (GT) is an autosomal recessive bleeding disorder which is due to a defect in platelet aggregation in response to multiple physiological agonists. It has been demonstrated that the clinical phenotype of various diseases inherited in a classic Mendelian fashion can be modulated by a series of factors, inherited as well as acquired.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1873-3492
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
403
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
156-8
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pubmed:meshHeading |
pubmed-meshheading:19245802-Antigens, Human Platelet,
pubmed-meshheading:19245802-Blood Coagulation Factors,
pubmed-meshheading:19245802-Blood Transfusion,
pubmed-meshheading:19245802-Epistaxis,
pubmed-meshheading:19245802-Fibrinogen,
pubmed-meshheading:19245802-Homozygote,
pubmed-meshheading:19245802-Humans,
pubmed-meshheading:19245802-Mutation,
pubmed-meshheading:19245802-Phenotype,
pubmed-meshheading:19245802-Platelet Aggregation,
pubmed-meshheading:19245802-Polymorphism, Genetic,
pubmed-meshheading:19245802-Thrombasthenia
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pubmed:year |
2009
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pubmed:articleTitle |
Modulation of clinical phenotype of Glanzmann's thrombasthenia by thrombogenic mutations.
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pubmed:affiliation |
Department of Hematology, All India Institute of Medical Sciences, New Delhi, India.
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pubmed:publicationType |
Journal Article
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