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Report on a disease-adapted treatment in a patient with severe factor X deficiency resulting from a homozygous factor X gene mutation.

Thrombosis and haemostasis - 1 Jan 2008

Gerhardt Andrea, Araba Fatima, Scharf Rüdiger E, Zotz Rainer B

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 18217161
DOI: 10.1160/TH07-08-0486

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Report on a disease-adapted treatment in a patient with severe factor X deficiency resulting from a homozygous factor X gene mutation.PMID 18217161Read ↗

Identification of a novel factor X deletion in combination with a missense mutation in the F10 gene - Genotype-phenotype correlation in a girl with severe factor X deficiency.Semantic proximity Read ↗

Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment.Semantic proximity Read ↗

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