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Article

Inherited protein S deficiency as a result of a large duplication mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification.

Journal of thrombosis and haemostasis : JTH - 1 Aug 2008

Choung H-S, Kim H-J, Gwak G-Y, Kim S-H, Kim D-K

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18489710
DOI: 10.1111/j.1538-7836.2008.03026.x

Genes

PROS1

Provenance

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Related research

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Inherited protein S deficiency as a result of a large duplication mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification.PMID 18489710Read ↗

Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA).Semantic proximity Read ↗

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Genotype and laboratory and clinical phenotypes of protein s deficiency.Semantic proximity Read ↗

Compound heterozygous mutations in the PROS1 gene responsible for quantitative and qualitative protein S deficiency.Semantic proximity Read ↗

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Large deletions of the PROS1 gene in a large fraction of mutation-negative patients with protein S deficiency.Semantic proximity Read ↗

Protein S Erlangen: a novel PROS1 gene mutation associated with quantitative protein S deficiency.Semantic proximity Read ↗

Protein S deficiency: a database of mutations--summary of the first update.Semantic proximity Read ↗

Late onset thrombosis in a case of severe protein S deficiency due to compound heterozygosity for PROS1 mutations.Semantic proximity Read ↗

A novel rare c.-39C>T mutation in the PROS1 5'UTR causing PS deficiency by creating a new upstream translation initiation codon.Semantic proximity Read ↗

The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population.Semantic proximity Read ↗

Molecular basis of protein S deficiency in ChinaSemantic proximity Read ↗

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