Human ARHGEF9 intellectual disability syndrome is phenocopied by a mutation that disrupts collybistin binding to the GABA(A) receptor α2 subunit

人类 ARHGEF9 智力障碍综合征的表型可由一种破坏 collybistin 与 GABA(A) 受体 α2 亚基结合的突变所模拟。