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Genetic analysis of a pedigree with hereditary coagulation factor XII deficiency

2024-10-17

Abstract excerpt

<title>Abstract</title> <p><bold>Objective: </bold>Analyze the clinical phenotype and gene mutations of a family with hereditary FXII deficiency, and preliminarily explore its molecular pathogenic mechanism. <bold>Methods:</bold> The routine coagulation indicators and related coagulation factors were measured.. Thromboelastography and thrombin generation tests simulated coagulation and anticoagulation states in v...

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Literature Corpus work
29d0f3dc-c3a2-5854-9789-dcf17ccf6867
DOI
10.21203/rs.3.rs-4978926/v1
Open publication

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Genetic analysis of a pedigree with hereditary coagulation factor XII deficiencyDOI 10.21203/rs.3.rs-4978926/v1
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