Coincidence of Wilson's disease with other movement disorders in the same family.
作者信息
Quinn N P, Marsden C D
出版信息
J Neurol Neurosurg Psychiatry. 1986 Feb;49(2):221-2. doi: 10.1136/jnnp.49.2.221.
Abstract
摘要
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Coincidence of Wilson's disease with other movement disorders in the same family.威尔逊氏病与同一家族中的其他运动障碍并存。
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Middle-aged heterozygous carriers of Wilson's disease do not present with significant phenotypic deviations related to copper metabolism.中年威尔逊病杂合子携带者未出现与铜代谢相关的明显表型偏差。
J Genet. 2010 Dec;89(4):463-7. doi: 10.1007/s12041-010-0065-3.
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Ceruloplasmin and superoxide dismutase (SOD1) in heterozygotes for Wilson disease: A case control study.血清铜蓝蛋白和超氧化物歧化酶 1（SOD1）在威尔逊病杂合子中的研究：一项病例对照研究。
Neuropsychiatr Dis Treat. 2009;5:55-9. doi: 10.2147/ndt.s4360. Epub 2009 Apr 8.
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Movement disorder associated with abnormal copper metabolism and decreased blood antioxidants.与铜代谢异常和血液抗氧化剂减少相关的运动障碍。
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Hereditary whispering dysphonia.遗传性低语性发声障碍
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