دورية أكاديمية

Loss-of-function mutation in PRMT9 causes abnormal synapse development by dysregulation of RNA alternative splicing

التفاصيل البيبلوغرافية
العنوان: Loss-of-function mutation in PRMT9 causes abnormal synapse development by dysregulation of RNA alternative splicing
المؤلفون: Shen, Lei, Ma, Xiaokuang, Wang, YuanyuanAff3, Aff4, Wang, Zhihao, Zhang, Yi, Pham, Hoang Quoc HaiAff1, Aff5, Tao, XiaoqunAff1, Aff5, Cui, Yuehua, Wei, Jing, Lin, Dimitri, Abeywanada, Tharindumala, Hardikar, Swanand, Halabelian, Levon, Smith, Noah, Chen, Taiping, Barsyte-Lovejoy, Dalia, Qiu, ShenfengAff2, IDs41467024471079_cor17, Xing, YiAff4, Aff8, Aff9, IDs41467024471079_cor18, Yang, YanzhongAff1, Aff5, IDs41467024471079_cor19
المصدر: Nature Communications. 15(1)
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:20411723
DOI:10.1038/s41467-024-47107-9