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NHP2
Wednesday 13 April 2016
Pathology
Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita. (18523010)
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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. Proc Natl Acad Sci U S A. 2008 Jun 10;105(23):8073-8. doi : 10.1073/pnas.0800042105 PMID: 18523010 (Free)