Open AccessCongenital factor V deficiency from compound heterozygous mutations with a novel variant c.2426del (p.Pro809Hisfs∗2) in the F5 gene
Author(s) -
Chang-Hun Park,
MinSeung Park,
Ki-O Lee,
SunHee Kim,
Young Shil Park,
HeeJin Kim
Publication year - 2020
Publication title -
medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 148
eISSN - 1536-5964
pISSN - 0025-7974
DOI - 10.1097/md.0000000000018947
Subject(s) - missense mutation , medicine , compound heterozygosity , partial thromboplastin time , factor v , mutation , genotype , heterozygote advantage , genetics , gene , gene mutation , genetic testing , gastroenterology , microbiology and biotechnology , coagulation , biology , thrombosis
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