Identification of vulnerable interneuron subtypes in 15q13.3 microdeletion syndrome using single-cell transcriptomics

A number of rare copy-number variants (CNVs) have been linked to neurodevelopmental disorders. However, since CNVs encompass many genes, it is often difficult to identify the mechanisms that lead to developmental perturbations.

Source: Biological Psychiatry - September 23, 2021 Category: Psychiatry Authors: Susmita Malwade, Janina Gasthaus, Carmelo Bellardita, Matej Andelic, Borna Moric, Irina Korshunova, Ole Kiehn, Navneet A. Vasistha, Konstantin Khodosevich Tags: Archival Report Source Type: research