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Article

A novel protein S gene mutation combined with protein S Tokushima mutation in a patient with superior sagittal sinus thrombosis.

Journal of neurology - 1 Jan 2012

Shindo Akihiro, Ikejiri Makoto, Ii Yuichiro, Nakatani Kaname, Wada Hideo, Nobori Tsutomu, Tomimoto Hidekazu

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 21647728
DOI: 10.1007/s00415-011-6122-x

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A novel protein S gene mutation combined with protein S Tokushima mutation in a patient with superior sagittal sinus thrombosis.PMID 21647728Read ↗

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One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.Semantic proximity Read ↗

[Hereditary protein S deficiency in a patient with prominent mesenteric venous thrombosis: A case report].Semantic proximity Read ↗

Racial differences in protein S Tokushima and two protein C variants as genetic risk factors for venous thromboembolismSemantic proximity Read ↗

A novel splice acceptor site mutation of protein S gene in affected individuals with type I protein S deficiency: allelic exclusion of the mutant gene.Semantic proximity Read ↗

[PROSI Mutation With Clinical Heterogeneity in Protein S Deficiency:Report of One Case].Semantic proximity Read ↗

Genotyping analysis of protein S-Tokushima (K196E) and the involvement of protein S antigen and activity in patients with recurrent pregnancy loss.Semantic proximity Read ↗

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