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Male‐specific alterations in structure of isolation call sequences of mouse pups with 16p11.2 deletion
16p11.2 deletion is one of the most common gene copy variations that increases the susceptibility to autism and other neurodevelopmental disorders. This syndrome leads to developmental delays, including speech impairment and delays in expressive language and communication skills. To study developmen...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Blackwell Publishing Ltd
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7116069/ https://www.ncbi.nlm.nih.gov/pubmed/32558237 http://dx.doi.org/10.1111/gbb.12681 |