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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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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists Limited
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3917245/ https://ncbi.nlm.nih.gov/pubmed/24357327 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.012484 |
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