TY  - GEN 
AU  - Rodríguez Heras, Sara
AU  - Colomer-Boronat, Ana
AU  - Peris Ripollés, Guillermo
AU  - Sánchez, Laura
AU  - Tristán Ramos, Pablo
AU  - Gázquez Gutiérrez, Ana
AU  - Barturen, Guillermo
AU  - Sánchez-Luque, Franscisco J.
AU  - García Pérez, José Luis
AU  - Macías, Sara
AU  - Rodríguez Heras, Sara
PY  - 2025
UR  - https://hdl.handle.net/10481/103305
AB  - The 22q11.2 deletion syndrome (22qDS) is a human disorder where the majority of clinical manifestations originate during embryonic development. 22qDS is caused by a microdeletion
in one chromosome 22, including DGCR8, an essential gene for miRNA...
LA  - eng
PB  - Oxford University Press
TI  - DGCR8 haploinsufficiency leads to primate-specific RNA dysregulation and pluripotency defects
DO  - 10.1093/nar/gkaf197
ER  -