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将一个导致非特异性智力迟钝(MRX9)的基因定位到X染色体的着丝粒周围区域。

Localization of a gene responsible for nonspecific mental retardation (MRX9) to the pericentromeric region of the X chromosome.

作者信息

Willems P, Vits L, Buntinx I, Raeymaekers P, Van Broeckhoven C, Ceulemans B

机构信息

Department of Medical Genetics, University of Antwerp-UIA, Belgium.

出版信息

Genomics. 1993 Nov;18(2):290-4. doi: 10.1006/geno.1993.1468.

Abstract

Nonspecific X-linked mental retardation (MRX) includes several distinct entities with mental retardation but without additional distinguishing features. The MRX family reported here has been classified previously as MRX9. In this study, we performed linkage analysis of MRX9 with a panel of 43 polymorphic DNA markers dispersed over chromosome X. Two-point linkage analysis revealed lod scores of 3.52 and 3.82 at 0% recombination for OATL1 and MAOA, both located in Xp11.2-p11.4. Lod scores for linkage with PGK1P1, DXS106, and DXS132, all located in Xq11-q13, were 3.83, 3.82, and 3.52, respectively, all at 0% recombination. Multipoint linkage analysis showed two peaks with MAOA and DXS132/DXS106, respectively. Analysis of recombinational events indicated a position of the MRX9 gene between DXS164 and DXS453. These findings are compatible with a location of the MRX9 gene in the pericentromeric region of the X chromosome at Xp21-q13.

摘要

非特异性X连锁智力迟钝(MRX)包括几种不同的智力迟钝类型,但无其他明显特征。本文报道的MRX家系先前被归类为MRX9。在本研究中,我们用一组分布于X染色体上的43个多态性DNA标记对MRX9进行连锁分析。两点连锁分析显示,位于Xp11.2-p11.4的OATL1和MAOA在0%重组率时的对数优势分数分别为3.52和3.82。位于Xq11-q13的PGK1P1、DXS106和DXS132的连锁对数优势分数分别为3.83、3.82和3.52,均在0%重组率时。多点连锁分析分别显示MAOA和DXS132/DXS106有两个峰值。重组事件分析表明MRX9基因位于DXS164和DXS453之间。这些发现与MRX9基因位于X染色体着丝粒周围区域Xp21-q13一致。

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