A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1
小鼠层粘连蛋白β1亚基Lamb1基因突变会导致一种类似肌张力障碍的运动障碍，并伴有脑和脊髓神经元缺陷。
期刊:Elife
影响因子:6.4
doi:10.7554/eLife.11102
Liu, Yi Bessie; Tewari, Ambika; Salameh, Johnny; Arystarkhova, Elena; Hampton, Thomas G; Brashear, Allison; Ozelius, Laurie J; Khodakhah, Kamran; Sweadner, Kathleen J
