Frequency of the p.Thr241Asn mutation in Chinese patients with congenital factor VII deficiency
Author:
Funder
Natural Science Foundation of Jiangxi Province
Publisher
Elsevier BV
Reference10 articles.
1. Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea;Kwon;Blood Coagul. Fibrinolysis,2011
2. Molecular analysis of the genotype-phenotype relationship in factor VII deficiency;Millar;Hum. Genet.,2000
3. Novel double heterozygous mutations on Met306Val and Thr181Asn related to a hereditary coagulation factor VII deficiency;Tu;Zhonghua Yi Xue Za Zhi,2006
4. Two novel factor VII gene mutations in a Chinese family with factor VII deficiency;Au;Br. J. Haematol.,2000
5. Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency;Ferraresi;Haematologica,2020
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1. Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients;Haemophilia;2024-05-23
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