Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects

Duncan, AR; Vitobello, A; Collins, SC; Vancollie, VE; Lelliott, CJ; Rodan, L; Shi, JH; Seman, AR; Agolini, E; Novelli, A; Prontera, P; Sacoto, MJG; Santiago-Sim, T; Trimouille, A; Goizet, C; Nizon, M; Bruel, AL; Philippe, C; Grant, PE; Wojcik, MH; Stoler, J; Genetti, CA; van Dooren, MF; Maas, SM; Alders, M; Faivre, L; Sorlin, A; Yoon, G; Yalcin, B; Agrawal, PB

Agrawal, PB (corresponding author), Boston Childrens Hosp, Dept Pediat, Div Newborn Med, Boston, MA 02115 USA.; Yalcin, B (corresponding author), Univ Bourgogne Franche Comte, INSERM UMR1231 Gad, F-21000 Dijon, France.; Agrawal, PB (corresponding author), Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA.; Agrawal, PB (corresponding author), Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Boston, MA 02115 USA.

AMERICAN JOURNAL OF HUMAN GENETICS, 2020; 107 (6): 1170