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Article

Retinal vasculopathy in autosomal dominant dyskeratosis congenita due to TINF2 mutation.

British journal of haematology - 1 Dec 2012

Gleeson Mary, O'Marcaigh Aengus, Cotter Melanie, Brosnahan Donal, Vulliamy Tom, Smith Owen P

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 23094712
DOI: 10.1111/bjh.12088

Genes

TINF2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Retinal findings and a novel TINF2 mutation in Revesz syndrome: Clinical and molecular correlations with pediatric retinal vasculopathies.Semantic proximity Read ↗

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