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Library » authors: Dokal I
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Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita.
Vulliamy T, Beswick R, Kirwan M, Marrone A, Digweed M, Walne A, Dokal I
Proceedings of National Academy of Sciences USA (2008)
Category: telomere ¤ Added: Jun 11th, 2008 ¤ Rating: ◊◊
Dyskeratosis congenita: telomerase, telomeres and anticipation.
Marrone A, Walne A, Dokal I
Current Opinion in Genetics and Development (2005)
Category: telomerase, telomere ¤ Added: May 30th, 2005 ¤ Rating: ◊◊