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Article

Cys482Trp missense mutation in the coagulation factor XI gene (F11) in a Korean patient with factor XI deficiency.

Annals of laboratory medicine - 1 Jul 2014

Choi Seung Jun, Kim Juwon, Lee Kyung-A, Choi Jong Rak, Yoo Jongha

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 24982842
DOI: 10.3343/alm.2014.34.4.332
PMCID: PMC4071194

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Related research

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Cys482Trp missense mutation in the coagulation factor XI gene (F11) in a Korean patient with factor XI deficiency.PMID 24982842Read ↗

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[Identification of compound heterozygous mutations p.Gly400Val and p.Arg532Ter of the F11 gene in a Chinese patient with hereditary factor XI deficiency].Semantic proximity Read ↗

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Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in China.Semantic proximity Read ↗

Genetic analysis in Factor XI deficient patients from central China: identification of one novel and seven recurrent mutations.Semantic proximity Read ↗

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Double Heterozygous Mutations (Cys247Tyr and 252delAsn) Cause Factor XII Deficiency in a Chinese Family.Semantic proximity Read ↗

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