Article

Lifespan in rodents with MYT1L heterozygous mutation

2024-11-03

Abstract excerpt

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. This model recapitulates several of the physical and neurologic abnormalities seen i...

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Literature Corpus work: 585ad9a6-a04e-5b8f-b503-b25ed625ec9d
DOI: 10.1101/2024.10.30.621094

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