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Familial typical migraine: significant linkage and localization of a gene to Xq24-28.

机译:家族性典型偏头痛:Xq24-28基因的显着连锁和定位。

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摘要

In a previous study we found evidence for an X-linked genetic component for familial typical migraine in two large Australian white pedigrees, designated MF7 and MF14. Significant excess allele sharing was indicated by nonparametric linkage (NPL) analysis using GENEHUNTER (P=0.031 and P=0.012, respectively), with a combined analysis of the two pedigrees showing further increased evidence for linkage, producing a maximum NPL score of 2.87 (P=0.011 ) at DXS 1123 on Xq27. The present study was aimed at refining the localization of the migraine X-chromosomal component by typing additional markers, performing haplotype analysis and applying a more powerful technique in the analysis of linkage data from these two pedigrees. Results from the haplotype analyses, coupled with linkage analyses that produced a peak GENEHUNTER-PLUS LOD* score of 2.388 (P=0.0005), provide compelling evidence for the presence of a migraine susceptibility locus on chromosome Xq24-28.
机译:在先前的研究中,我们发现了两个大型澳大利亚白人谱系(MF7和MF14)中典型家族性偏头痛的X连锁遗传成分的证据。使用GENEHUNTER的非参数连锁(NPL)分析表明存在明显的过量等位基因共享(分别为P = 0.031和P = 0.012),对两个谱系的组合分析显示连锁的证据进一步增加,产生的最大NPL得分为2.87( P = 0.011)在Xq27上的DXS 1123处。本研究旨在通过键入其他标记,进行单倍型分析并在分析来自这两个家谱的连锁数据中应用更强大的技术来完善偏头痛X染色体组件的定位。单倍型分析的结果,加上连锁分析得出的GENEHUNTER-PLUS LOD *峰值为2.388(P = 0.0005),为Xq24-28染色体上存在偏头痛敏感性位点提供了令人信服的证据。

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