Novel 14q32.2 paternal deletion encompassing the whole DLK1 gene associated with Temple syndrome

Temple syndrome (TS14) is a rare imprinting disorder caused by maternal UPD14, imprinting defects or paternal microdeletions which lead to an increase in the maternal expressed genes and a silencing the patern...

Source: Clinical Epigenetics - May 7, 2024 Category: Research Authors: Neus Baena, David Monk, Cinthia Aguilera, Mario F. Fraga, Agust ín F. Fernández, Elisabeth Gabau, Raquel Corripio, Nuria Capdevila, Juan Pablo Trujillo, Anna Ruiz and Miriam Guitart Tags: Research Source Type: research