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研究人员对导致铁在基底神经节沉积的两个基因突变的发现,为了解两种罕见的遗传性神经变性疾病提供了一个巨大的飞跃。美国俄勒冈州立卫生科学大学的Susan Hatflick说,人们从临床和疾病的病理学开始到阐述描绘疾病状况的探子和对疾病发病机制的可试验假说,直至提出可能的治疗方法几乎是在一夜间完成的。
The discovery of two genetic mutations that lead to the deposition of iron in the basal ganglia has provided a huge leap forward in understanding two rare hereditary neurodegenerative diseases. Susan Hatflick of Oregon State University of Health Sciences, in the US, says people start with clinical and pathological pathology to describe testable spirits that describe disease conditions and testable hypotheses on the pathogenesis of the disease until possible treatment is proposed almost overnight .