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...
| 出版年: | BMC Medicine |
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| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | 論文 |
| 言語: | 英語 |
| 出版事項: |
BMC
2024-04-01
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| 主題: | |
| オンライン・アクセス: | https://doi.org/10.1186/s12916-024-03363-6 |
