Associated Papers
Utility of whole genome sequencing in assessing risk and clinically relevant outcomes for pulmonary fibrosis.
Zhang D et al.
The European Respiratory Journal, 2022
TERT and TERC mutations detected in cryptic dyskeratosis congenita suppress telomerase activity.
Terada K et al.
International Journal of Laboratory Hematology, 2020
Clinical and genetic features of dyskeratosis congenita, cryptic dyskeratosis congenita, and Hoyeraal-Hreidarsson syndrome in Japan.
Yamaguchi H et al.
International Journal of Hematology, 2015
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