Abstract
Herein, a neonate with congenital FVII deficiency is presented. Diagnosis of congenital FVII deficiency was confirmed by genetic analysis using next-generation sequencing method (MiSeq-Illumina). Our patient was found to have a novel homozygous mutation. Early diagnosis and treatment of congenital FVII deficiency can be crucial.
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Schedule a callMore From: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
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