Olfactory bulb anomalies in KBG syndrome mouse model and patients
Abstract ANKRD11 (ankyrin repeat domain 11) is a chromatin regulator and the only gene associated with KBG syndrome, a rare neurodevelopmental disorder. We have previously shown that Ankrd11 regulates murine embryonic cortical neurogenesis. Here, we show a novel olfactory bulb phenotype in a KBG syn...
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| Hauptverfasser: | , , , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMC
2024-04-01
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| Schriftenreihe: | BMC Medicine |
| Schlagworte: | |
| Online-Zugang: | https://doi.org/10.1186/s12916-024-03363-6 |
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