Disrupted Coordination of Hypoglossal Motor Control in a Mouse Model of Pediatric Dysphagia in DiGeorge/22q11.2 Deletion Syndrome

We asked whether the physiological and morphologic properties of hypoglossal motor neurons (CNXII MNs) that innervate protruder or retractor tongue muscles are disrupted in neonatal LgDel mice that carry a heterozygous deletion parallel to that associated with DiGeorge/22q11.2 deletion syndrome (22q...

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Vydáno v:eNeuro
Hlavní autoři: Wang, Xin, Popratiloff, Anastas, Motahari, Zahra, LaMantia, Anthony-Samuel, Mendelowitz, David
Médium: Artigo
Jazyk:Inglês
Vydáno: Society for Neuroscience 2020
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Research Article: New Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7548433/
https://ncbi.nlm.nih.gov/pubmed/32855199
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/ENEURO.0520-19.2020
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