Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome
Volume
19
Pagination
4453 - 4461
DOI
10.1093/hmg/ddq371
Journal
HUM MOL GENET
Issue
ISSN
0964-6906