De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in females
Dong Li, Alanna Strong, Kaitlyn M Shen, David Cassiman, Maria Van Dyck, Natália D. Linhares, Eugênia Ribeiro Valadares, Tian-Cheng Wang, Sérgio D.J. Pena, Jaak Jaeken, Samantha A. Schrier Vergano, Elaine H. Zackai, Anne Hing, Penny Chow, Arupa Ganguly, Tasja Scholz, Tatjana Bierhals, Philipp Deindl, Håkon Håkonarson, Elizabeth Bhoj
Topics & Concepts
Frameshift mutationNonsenseIntellectual disabilityExome sequencingGeneticsPhenotypeMedicineMissense mutationGlobal developmental delayLoss functionMedical geneticsBiologyGenePediatric Hepatobiliary Diseases and TreatmentsEsophageal and GI PathologyConnective tissue disorders research