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...

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Detalles Bibliográficos
Autores principales: Agarwalla, Swapna, Arroyo, Noelle S., Long, Natalie E., O'Brien, William T., Abel, Ted, Bandyopadhyay, Sharba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2020
Materias:
Original Articles
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

Internet

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

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