Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome

Disrupted development of oropharyngeal structures as well as cranial nerve and brainstem circuits may lead to feeding and swallowing difficulties in children with 22q11. 2 deletion syndrome (22q11DS). We previously demonstrated aspiration-based dysphagia during early postnatal life in the LgDel mous...

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Detalles Bibliográficos
Autores principales: Welby, Lauren, Caudill, Hailey, Yitsege, Gelila, Hamad, Ali, Bunyak, Filiz, Zohn, Irene E., Maynard, Thomas, LaMantia, Anthony-Samuel, Mendelowitz, David, Lever, Teresa E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006055/
https://www.ncbi.nlm.nih.gov/pubmed/32082240
http://dx.doi.org/10.3389/fneur.2020.00004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006055/
https://www.ncbi.nlm.nih.gov/pubmed/32082240
http://dx.doi.org/10.3389/fneur.2020.00004

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