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...

詳細記述

書誌詳細
出版年:BMC Medicine
主要な著者: Kara Goodkey, Anita Wischmeijer, Laurence Perrin, Adrianne E. S. Watson, Leenah Qureshi, Duccio Maria Cordelli, Francesco Toni, Maria Gnazzo, Francesco Benedicenti, Monique Elmaleh-Bergès, Karen J. Low, Anastassia Voronova
フォーマット: 論文
言語:英語
出版事項: BMC 2024-04-01
主題:
オンライン・アクセス:https://doi.org/10.1186/s12916-024-03363-6