Roles of NRXN1 in neuropsychiatric disorders: from genetic lesion to molecular mechanism
Numerous neuropsychiatric disorders frequently exhibit overlapping genetic risk factors, implying the molecular basis for their comorbidity. Nevertheless, the pathogenesis of these disorders remains elusive, particularly regarding how genetic variations impair the physiological function of risk gene...
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| Glavni autori: | , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Frontiers Media S.A.
2026-05-01
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| Serija: | Frontiers in Neuroscience |
| Teme: | |
| Online pristup: | https://www.frontiersin.org/articles/10.3389/fnins.2026.1808921/full |
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