Lifespan in rodents with MYT1L heterozygous mutation

Abstract MYT1L syndrome is a newly recognized disorder characterized by intellectual disability, speech and motor delay, neuroendocrine disruptions, ADHD, and autism. In order to study this gene and its association with these phenotypes, our lab recently created a Myt1l heterozygous mutant mouse ins...

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Bibliographic Details
Published in:	Scientific Reports
Main Authors:	Allyson Schreiber, Raylynn G. Swift, Leslie Wilson, Kristen L. Kroll, Joseph D. Dougherty, Susan E. Maloney
Format:	Article
Language:	English
Published:	Nature Portfolio 2025-02-01
Subjects:	Lifespan Obesity MYT1L syndrome Neurodevelopmental disorders
Online Access:	https://doi.org/10.1038/s41598-025-88462-x

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