Three novel truncating TINF2 mutations causing severe dyskeratosis congenita in early childhood

Sasa GS, Ribes-Zamora A, Nelson ND, Bertuch AA. Three novel truncating TINF2 mutations causing severe dyskeratosis congenita in early childhood. Clin Genet. 2012 May;81(5):470-8.

PubMed ID: 
21477109