Novel TINF2 gene mutation in dyskeratosis congenita with extremely short telomeres: A case report.
Picos-Cárdenas VJ, Beltrán-Ontiveros SA, Cruz-Ramos JA, Contreras-Gutiérrez JA, Arámbula-Meraz E, Angulo-Rojo C, Guadrón-Llanos AM, Leal-León EA, Cedano-Prieto DM, Meza-Espinoza JP.
Picos-Cárdenas VJ, et al. Among authors: meza espinoza jp.
World J Clin Cases. 2022 Nov 26;10(33):12440-12446. doi: 10.12998/wjcc.v10.i33.12440.
World J Clin Cases. 2022.
PMID: 36483815
Free PMC article.