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Article

The factor VIII gene intron 1 inversion mutation: prevalence in severe hemophilia A patients in the UK

1 Jan 2004

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 14717992
DOI: 10.1111/j.1538-7836.2004.0562i.x

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The factor VIII gene intron 1 inversion mutation: prevalence in severe hemophilia A patients in the UKPMID 14717992Read ↗

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Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.Semantic proximity Read ↗

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Factor VIII gene inversions in severe hemophilia A patients.Semantic proximity Read ↗

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[Frequency of intron 1 inversion of factor VIII gene in Chinese hemophilia A patients with case report of a female patient with heterozygous intron 1 inversion].Semantic proximity Read ↗

Identification of deep intronic individual variants in patients with hemophilia A by next‐generation sequencing of the whole factor VIII geneSemantic proximity Read ↗

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