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Retinal vasculopathy in autosomal dominant dyskeratosis congenita due to TINF 2 mutation
Author(s) -
Gleeson Mary,
O'Marcaigh Aengus,
Cotter Melanie,
Brosnahan Donal,
Vulliamy Tom,
Smith Owen P.
Publication year - 2012
Publication title -
british journal of haematology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/bjh.12088
Subject(s) - dyskeratosis congenita , fundus (uterus) , medicine , retina , retinal , visual acuity , ophthalmology , fluorescein angiography , dyskeratosis , pathology , biology , genetics , telomere , hyperkeratosis , gene , neuroscience
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