VIB Center for the Biology of Disease, 3000 Leuven, Belgium; Center for Human Genetics and Leuven Institute for Neurodegenerative Diseases (LIND), KU Leuven, 3000 Leuven, Belgium.
VIB Center for the Biology of Disease, 3000 Leuven, Belgium; Center for Human Genetics and Leuven Institute for Neurodegenerative Diseases (LIND), KU Leuven, 3000 Leuven, Belgium; Department of Biomedicine and Prevention, University of Rome "Tor Vergata," 00133 Rome, Italy.
Cell. 2014 Sep 25;159(1):218-218.e1. doi: 10.1016/j.cell.2014.08.036.
The Fragile X syndrome, caused by the absence or mutation of fragile X mental retardation protein, FMRP, is a the common component of inherited intellectual disability and autism. This SnapShot surveys the protein interaction partners of FMRP, focusing on the cellular pathways in which they are involved.
脆性 X 综合征是由脆性 X 智力迟钝蛋白 FMRP 的缺失或突变引起的，是遗传性智力残疾和自闭症的常见组成部分。这个 SnapShot 调查了 FMRP 的蛋白质相互作用伙伴，重点关注它们所涉及的细胞途径。
