Aberrant early growth of individual trigeminal sensory and motor axons in a series of mouse genetic models of 22q11.2 deletion syndrome.

Hum Mol Genet · 2020 · PMC7645708 · PMID 32901287

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0.8800

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0.8800

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did not reach statistical significanceP = 0.88not close (p > 0.1)

The scored phenotypes, branching and misrouting, were slightly elevated in LgDel +/− CN V sensory ( n = 43) versus WT sensory ( n = 30) axons; however, this increase did not reach statistical significance ( P = 0.88; Fisher Exact/Chi Square; Fig. 5H , left ).

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