Article

Lifespan in rodents with MYT1L heterozygous mutation

2024-12-17

Abstract excerpt

<title>Abstract</title> <p>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 <italic>Myt1l</italic> heterozygous mutant mouse inspired by a clinically relevant mutation. This model recapitulates several of the...

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Literature Corpus work: 90269a8d-4163-5392-b0d6-8a1aa18217cf
DOI: 10.21203/rs.3.rs-5140229/v1

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