Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects
Anna R. Duncan, Antonio Vitobello, Stephan C. Collins, Valerie E. Vancollie, Christopher J. Lelliott, Lance H. Rodan, Jiahai Shi, Ann R. Seman, Emanuele Agolini, Antonio Novelli, Paolo Prontera, María J. Guillen Sacoto, Teresa Santiago‐Sim, Aurélien Trimouille, Cyril Goizet, Mathilde Nizon, Ange‐Line Bruel, Christophe Philippe, P. Ellen Grant, Monica H. Wojcik, Joan M. Stoler, Casie A. Genetti, Marieke F. van Dooren, Saskia M. Maas, Mariëlle Alders, Laurence Faivre, Arthur Sorlin, Grace Yoon, Binnaz Yalcin, Pankaj B. Agrawal
Topics & Concepts
BiologyCorpus callosumAgenesis of the corpus callosumNeuroscienceVentriculomegalyGlobal developmental delayPolymicrogyriaGeneticsEpilepsyGenePhenotypeFetusPregnancyEpigenetics and DNA MethylationGenetics and Neurodevelopmental DisordersGenetic Syndromes and Imprinting