Open AccessExpanding the clinical phenotype of autosomal dominant dyskeratosis congenita caused by TERT mutations
Author(s) -
Lina BaselVanagaite,
Inderjeet Dokal,
Hannah Tamary,
Abraham Avigdor,
Ben Zion Garty,
Alexander Volkov,
Tom Vulliamy
Publication year - 2008
Publication title -
haematologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.782
H-Index - 142
eISSN - 1592-8721
pISSN - 0390-6078
DOI - 10.3324/haematol.12317
Subject(s) - dyskeratosis congenita , phenotype , genetics , mutation , clinical phenotype , dyskeratosis , genodermatosis , biology , medicine , dermatology , telomere , hyperkeratosis , gene