Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome

We assessed feeding-related developmental anomalies in the LgDel mouse model of chromosome 22q11 deletion syndrome (22q11DS), a common developmental disorder that frequently includes perinatal dysphagia – debilitating feeding, swallowing and nutrition difficulties from birth onward – within its phen...

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Detalles Bibliográficos
Autores principales: Karpinski, Beverly A., Maynard, Thomas M., Fralish, Matthew S., Nuwayhid, Samer, Zohn, Irene E., Moody, Sally A., LaMantia, Anthony-S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Limited 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917245/
https://www.ncbi.nlm.nih.gov/pubmed/24357327
http://dx.doi.org/10.1242/dmm.012484

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917245/
https://www.ncbi.nlm.nih.gov/pubmed/24357327
http://dx.doi.org/10.1242/dmm.012484

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