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日本血清铜蓝蛋白缺乏症基因频率的估计。

Estimation of the gene frequency of aceruloplasminemia in Japan.

作者信息

Miyajima H, Kohno S, Takahashi Y, Yonekawa O, Kanno T

机构信息

First Department of Medicine, Hamamatsu University School of Medicine, Japan.

出版信息

Neurology. 1999 Aug 11;53(3):617-9. doi: 10.1212/wnl.53.3.617.

Abstract

Aceruloplasminemia is a newly recognized autosomal recessive disorder of iron metabolism that causes neurodegeneration of the retina and basal ganglia as well as diabetes mellitus. We screened the serum ceruloplasmin concentrations of 4,990 healthy adult individuals. Subsequent sequence determination of the mutant alleles showed three mutations (5-bp insertion in exon 7, one heterozygote, one-bp deletion in exon 14, two heterozygotes, nonsense mutation in exon 15, one homozygote and two heterozygotes). The gene frequency was 70/100,000. In Japan, the incidence of aceruloplasminemia was estimated to be approximately 1 per 2,000,000 in the case of nonconsanguineous marriages.

摘要

无铜蓝蛋白血症是一种新发现的常染色体隐性铁代谢紊乱疾病,可导致视网膜和基底神经节神经退行性变以及糖尿病。我们检测了4990名健康成年人的血清铜蓝蛋白浓度。随后对突变等位基因进行测序,发现了三种突变(外显子7有5个碱基对插入,1个杂合子;外显子14有1个碱基对缺失,2个杂合子;外显子15有一个无义突变,1个纯合子和2个杂合子)。基因频率为70/100,000。在日本,非近亲结婚情况下无铜蓝蛋白血症的发病率估计约为每2,000,000人中有1例。

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