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...
में बचाया:
| मुख्य लेखकों: | , , , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
The Company of Biologists
2014-02-01
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| श्रृंखला: | Disease Models & Mechanisms |
| विषय: | |
| ऑनलाइन पहुंच: | http://dmm.biologists.org/content/7/2/245 |
| टैग: |
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