A mutation in a functional Sp1 binding site of the telomerase RNA gene (hTERC) promoter in a patient with Paroxysmal Nocturnal Haemoglobinuria

BACKGROUND: Mutations in the gene coding for the RNA component of telomerase, hTERC, have been found in autosomal dominant dyskeratosis congenita (DC) and aplastic anemia. Paroxysmal nocturnal hemoglobinuria (PNH) is a clonal blood disorder associated with aplastic anemia and characterized by the pr...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Keith, W Nicol, Vulliamy, Tom, Zhao, Jiangqin, Ar, Cem, Erzik, Can, Bilsland, Alan, Ulku, Birsen, Marrone, Anna, Mason, Philip J, Bessler, Monica, Serakinci, Nedime, Dokal, Inderjeet
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2004
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC442127/
https://ncbi.nlm.nih.gov/pubmed/15212690
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2326-4-3
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados