Whole genome investigation of an atypical autism case identifies a novel ANOS1 mutation with subsequent diagnosis of Kallmann syndrome

Publication date: June 2020Source: Molecular Genetics and Metabolism Reports, Volume 23Author(s): Paul A. Dawson, Soohyun Lee, Adam D. Ewing, Johannes B. Prins, Helen S. Heussler

Source: Molecular Genetics and Metabolism Reports - April 30, 2020 Category: Genetics & Stem Cells Source Type: research