The phenotypic and genetic assessment of antithrombin deficiency.
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Clinical Scenarios for Discordant Anti-XaA small deletion in SERPINC1 causes type I antithrombin deficiency by promoting endoplasmic reticulum stress.Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect.A complex genomic abnormality found in a patient with antithrombin deficiency and autoimmune disease-like symptoms.Molecular basis of coronary artery dilation and aneurysms in patients with Kawasaki disease based on differential protein expression.Assessment of Hereditary Thrombophilia: Performance of Antithrombin (AT) Testing.
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The phenotypic and genetic assessment of antithrombin deficiency.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 15 March 2011
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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name
The phenotypic and genetic assessment of antithrombin deficiency.
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The phenotypic and genetic assessment of antithrombin deficiency.
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type
label
The phenotypic and genetic assessment of antithrombin deficiency.
@en
The phenotypic and genetic assessment of antithrombin deficiency.
@nl
prefLabel
The phenotypic and genetic assessment of antithrombin deficiency.
@en
The phenotypic and genetic assessment of antithrombin deficiency.
@nl
P2093
P2860
P1476
The phenotypic and genetic assessment of antithrombin deficiency.
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P2093
P2860
P304
P356
10.1111/J.1751-553X.2011.01307.X
P577
2011-03-15T00:00:00Z