Martina Minnerop, Delia Kurzwelly, Holger Wagner, Anne S. Soehn, Jennifer Reichbauer, Feifei Tao, et al. Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia. Brain 2017; 140: 1561–1578, https://doi.org/10.1093/brain/awx095.

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Martina Minnerop，Delia Kurzwelly，Holger Wagner，Anne S.Soehn，Jennifer Reichbauer，Feifei Tao等。在亚等位基因突变POLR3A是零星的，隐性的性痉挛性共济失调的常见原因。脑2017; 140：1561-1578，https：//doi.org/10.1093/brain/awx095。