Comprehensive Behavioral Phenotyping of a 16p11.2 Del Mouse Model for Neurodevelopmental Disorders
Sign Up to like & getrecommendations! Published in 2020 at "Autism Research"
DOI: 10.1002/aur.2357
Abstract: The microdeletion of copy number variant 16p11.2 is one of the most common genetic mutations associated with neurodevelopmental disorders, such as Autism Spectrum Disorders (ASDs). Here, we describe our comprehensive behavioral phenotyping of the 16p11.2… read more here.
Keywords: phenotyping 16p11; behavioral phenotyping; delm males; neurodevelopmental disorders ... See more keywords