Loss of neuronal potassium/chloride cotransporter 3 (KCC3) is responsible for the degenerative phenotype in a conditional mouse model of hereditary motor and sensory neuropathy associated with agenesis of the corpus callosum
神经元钾/氯协同转运蛋白 3 (KCC3) 的缺失是导致与胼胝体发育不全相关的遗传性运动和感觉神经病条件小鼠模型出现退化表型的原因
期刊:Journal of Neuroscience
影响因子:4.4
doi:10.1523/JNEUROSCI.3679-11.2012
Masoud Shekarabi, Randal X Moldrich, Sarah Rasheed, Adéle Salin-Cantegrel, Janet Laganière, Daniel Rochefort, Pascale Hince, Karine Huot, Rébecca Gaudet, Nyoman Kurniawan, Susana G Sotocinal, Jennifer Ritchie, Patrick A Dion, Jeffrey S Mogil, Linda J Richards, Guy A Rouleau