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Article

Factor V Leiden mutation in association with idiopathic intracranial hypertension.

The British journal of ophthalmology - 1 Jul 1998

Backhouse O, Metcalfe T, Goulding P, McEvoy M, Menage M

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 9924388
DOI: 10.1136/bjo.82.7.841d
PMCID: PMC1722681

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Factor V Leiden mutation in association with idiopathic intracranial hypertension.PMID 9924388Read ↗

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Glycosylation type Ic disorder: idiopathic intracranial hypertension and retinal degeneration.Semantic proximity Read ↗

Association of factor V Leiden and prothrombin gene mutation with Behçet's disease.Semantic proximity Read ↗

Cerebral infarct associated with prothrombin gene G 20210 A variant in a Turkish child with cystic fibrosis: an unusual coexistence.Semantic proximity Read ↗

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