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Allyson Schreiber

As seen in: BioRxiv
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Articles

Lifespan in rodents with MYT1L heterozygous mutation

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By Raylynn G Swift, Leslie Wilson, Kristen L. Kroll, Allyson Schreiber
| BioRxiv
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 inspired by a clinically relevant mutation.
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