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

Authors

W Nicol Keith, University of Glasgow
Tom Vulliamy, Imperial College School of Medicine
Jiangqin Zhao, University of Glasgow
Cem Ar, Istanbul University
Can Erzik, Marmara University Istanbul
Alan Bilsland, University of Glasgow
Birsen Ulku, Istanbul University
Anna Marrone, Imperial College School of Medicine
Philip J. Mason, Imperial College School of Medicine
Monica Bessler, Washington University School of Medicine in St. Louis
Nedime Serakinci, University of Aarhus
Inderjeet Dokal, Imperial College School of Medicine

Journal

BMC Blood Disorders

Publication Date

2004

Volume

4

Inclusive Pages

3

Document Type

Open Access Publication

Rights and Permissions

BMC Blood Disorders 2004, 4:3 http://www.biomedcentral.com/1471-2326/4/3

Recommended Citation

Keith, W Nicol; Vulliamy, Tom; Zhao, Jiangqin; Ar, Cem; Erzik, Can; Bilsland, Alan; Ulku, Birsen; Marrone, Anna; Mason, Philip J.; Bessler, Monica; Serakinci, Nedime; and Dokal, Inderjeet, "A mutation in a functional Sp1 binding site of the telomerase RNA gene (hTERC) promoter in a patient with Paroxysmal Nocturnal Haemoglobinuria." BMC Blood Disorders. 4, 3. (2004).
https://digitalcommons.wustl.edu/open_access_pubs/128