Meehan Richard R, Pennings Sari
MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Centre for Cardiovascular Science, Institute for Neuroscience and Cardiovascular Research, University of Edinburgh, Edinburgh, EH16 4TJ, UK.
EMBO Mol Med. 2024 Dec;16(12):3030-3032. doi: 10.1038/s44321-024-00154-7. Epub 2024 Nov 4.
Rett syndrome is a severe neurodevelopmental disorder in girls, underpinned by mutations in the X-linked gene . In their recent work (Frasca et al, 2024), Frasca and colleagues identified a novel pathway involving interferon-gamma (IFNγ) that could pave the way to potential therapies.
雷特综合征是一种发生在女孩中的严重神经发育障碍,由X连锁基因的突变引起。在他们最近的研究工作中(弗拉斯卡等人,2024年),弗拉斯卡及其同事发现了一条涉及γ干扰素(IFNγ)的新途径,这可能为潜在的治疗方法铺平道路。