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...
| Published in: | Scientific Reports |
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| Main Authors: | , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-02-01
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| Subjects: | |
| Online Access: | https://doi.org/10.1038/s41598-025-88462-x |