Litcius/Paper detail

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

2020Genetics in Medicine34 citationsDOIOpen Access PDF

Topics & Concepts

Frameshift mutationNonsenseIntellectual disabilityExome sequencingGeneticsPhenotypeMedicineMissense mutationGlobal developmental delayLoss functionMedical geneticsBiologyGenePediatric Hepatobiliary Diseases and TreatmentsEsophageal and GI PathologyConnective tissue disorders research