Dyskeratosis congenita: its link to telo
β
Inderjeet Dokal; Tom Vulliamy
π
Article
π
2003
π
Elsevier Science
π
English
β 353 KB
Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome exhibiting considerable clinical and genetic heterogeneity. X-linked recessive, autosomal dominant and autosomal recessive forms are recognised. The gene mutated in X-linked DC (DKC1) encodes a highly conserved nucleolar protei