匈牙利血色素沉着症C282Y突变的高频率可能与该突变起源于凯尔特人相矛盾。 - Suppr

Suppr

超能文献

High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation.

作者信息

Tordai A, Andrikovics H, Kalmár L, Rajczy K, Pénzes M, Sarkadi B, Klein I, Váradi A

出版信息

J Med Genet. 1998 Oct;35(10):878-9. doi: 10.1136/jmg.35.10.878-a.

DOI:10.1136/jmg.35.10.878-a

PMID:9783719

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1051471/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec25/1051471/bcbea57a3eb3/jmedgene00239-0087-a.jpg

相似文献

High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation.匈牙利血色素沉着症C282Y突变的高频率可能与该突变起源于凯尔特人相矛盾。

J Med Genet. 1998 Oct;35(10):878-9. doi: 10.1136/jmg.35.10.878-a.

Frequency of the hemochromatosis C282Y and H63D mutations in a Polish population of Slavic origin.波兰斯拉夫人后裔群体中血色素沉着症C282Y和H63D突变的频率。

Med Sci Monit. 2001 May-Jun;7(3):441-3.

Frequency of the C282Y mutation of hemochromatosis in five French populations.

Blood Cells Mol Dis. 1998 Jun;24(2):165-6. doi: 10.1006/bcmd.1998.0183.

Prevalence of the C282Y mutation for haemochromatosis on the Island of Majorca.马略卡岛血色素沉着症C282Y突变的患病率。

Clin Genet. 2000 Aug;58(2):123-8. doi: 10.1034/j.1399-0004.2000.580206.x.

Celtic origin of the C282Y mutation of hemochromatosis.血色素沉着症C282Y突变的凯尔特起源。

Blood Cells Mol Dis. 1998 Dec;24(4):433-8. doi: 10.1006/bcmd.1998.0212.

Frequency analysis and allele map in favor of the celtic origin of the C282Y mutation of hemochromatosis.支持血色素沉着症C282Y突变具有凯尔特血统起源的频率分析和等位基因图谱。

Blood Cells Mol Dis. 2001 Mar-Apr;27(2):549-56. doi: 10.1006/bcmd.2001.0417.

Role of C282Y mutation in haemochromatosis gene in development of type 2 diabetes in healthy men: prospective cohort study.血色素沉着症基因中C282Y突变在健康男性2型糖尿病发生中的作用：前瞻性队列研究

BMJ. 2000 Jun 24;320(7251):1706-7. doi: 10.1136/bmj.320.7251.1706.

Haemochromatosis, HFE and genetic complexity.

Nat Genet. 1997 Dec;17(4):375-6. doi: 10.1038/ng1297-375.

[Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].[瑞士遗传性血色素沉着症患者中HFE基因突变频率及基因型-表型相关性]

Schweiz Med Wochenschr. 2000 Aug 8;130(31-32):1112-9.

The significance of the 187G (H63D) mutation in hemochromatosis.血色素沉着症中187G（H63D）突变的意义。

Am J Hum Genet. 1997 Sep;61(3):762-4.

引用本文的文献

The evolutionary adaptation of the C282Y mutation to culture and climate during the European Neolithic.欧洲新石器时代C282Y突变对文化和气候的进化适应。

Am J Phys Anthropol. 2016 May;160(1):86-101. doi: 10.1002/ajpa.22937. Epub 2016 Jan 22.

本文引用的文献

Absence of the hemochromatosis gene Cys282Tyr mutation in three ethnic groups from Algeria (Mzab), Ethiopia, and Senegal.来自阿尔及利亚（姆扎卜）、埃塞俄比亚和塞内加尔的三个种族群体中血色素沉着症基因Cys282Tyr突变的缺失。

Immunogenetics. 1997;46(3):222-5. doi: 10.1007/s002510050265.

Prevalence of hereditary hemochromatosis in a Massachusetts corporation: is Celtic origin a risk factor?

Hepatology. 1997 Jun;25(6):1439-46. doi: 10.1002/hep.510250622.

Global prevalence of putative haemochromatosis mutations.假定的血色素沉着症突变的全球患病率。

J Med Genet. 1997 Apr;34(4):275-8. doi: 10.1136/jmg.34.4.275.

Rapid diagnosis of the HLA-H gene Cys 282 Tyr mutation in hemochromatosis by polymerase chain reaction--a very rare mutation in the Chinese population.

Blood. 1997 May 1;89(9):3492-3.

Simple and rapid detection of the newly described mutations in the HLA-H gene.简单快速检测HLA-H基因中新发现的突变。

Blood. 1997 Mar 1;89(5):1835-6.

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.一种新的MHC I类样基因在遗传性血色素沉着症患者中发生突变。

Nat Genet. 1996 Aug;13(4):399-408. doi: 10.1038/ng0896-399.

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验