Litcius/Paper detail

Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt

James L. Shepherdson, Katie Hutchison, Dilan Wellalage Don, George McGillivray, Tae‐Ik Choi, Carolyn A Allan, David J. Amor, Siddharth Banka, Donald Basel, Laura D. Buch, Deanna Alexis Carere, Renée Carroll, Jill Clayton‐Smith, Ali Crawford, Morten Dunø, Laurence Faivre, Christopher P. Gilfillan, Nina B. Gold, Karen W. Gripp, Emma Hobson, Alexander M. Holtz, A. Micheil Innes, Bertrand Isidor, Adam Jackson, Panagiotis Katsonis, Leila Amel Riazat Kesh, Sébastien Küry, François Lecoquierre, Paul J. Lockhart, Julien Maraval, Naomichi Matsumoto, Julie McCarrier, Josephine McCarthy, Noriko Miyake, Lip Hen Moey, Andrea H. Németh, Elsebet Østergaard, Rushina Patel, Kate Pope, Jennifer E. Posey, Rhonda E. Schnur, Marie Shaw, Elliot Stolerman, Julie P. Taylor, Erin Wadman, Emma Wakeling, Susan M. White, Lawrence C. Wong, James R. Lupski, Olivier Lichtarge, Mark Corbett, Jozef Gécz, Charles M. Nicolet, Peggy Farnham, Cheol‐Hee Kim, Marwan Shinawi

2024The American Journal of Human Genetics18 citationsDOIOpen Access PDF

Topics & Concepts

BiologyGeneticsMissense mutationExome sequencingExomeHaploinsufficiencyIntellectual disabilityGermline mosaicismGermlineHypotoniaNeurodevelopmental disorderPhenotypeGeneGenetics and Neurodevelopmental DisordersCongenital heart defects researchGenomics and Rare Diseases