Indentification of novel MSTO1 compound heterozygous mutations in a Chinese family with recessive cerebellar atrophy and ataxia by Jia Chen, Junfang Xiao, Junfang Xiao, Ge Chen, Qiang Xu, Xingwu Wu, Lifeng Tian, Zhihui Huang, Cailin Xin, Yan Zhao, Zhen Guo, Yang Zou, Qiongfang Wu

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