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两种不同的X连锁视网膜色素变性基因。

Two different genes for X-linked retinitis pigmentosa.

作者信息

Wirth B, Denton M J, Chen J D, Neugebauer M, Halliday F B, van Schooneveld M, Donald J, Bleeker-Wagemakers E M, Pearson P L, Gal A

机构信息

Institut für Humangenetik, Medizinische Statistik der Universität, Bonn, Federal Republic of Germany.

出版信息

Genomics. 1988 Apr;2(3):263-6. doi: 10.1016/0888-7543(88)90011-0.

Abstract

Linkage analysis was carried out in three large multigenerational kindreds with X-linked retinitis pigmentosa using DNA markers on Xp. About 10% recombination has been found between the retinitis pigmentosa locus (RP2) and the marker locus DXS7, assigned to band Xp11.3, which was reported earlier to be closely linked to RP2 in several independent families. In the kindreds described in this paper, however, RP2 shows close linkage and no recombination with the marker loci OTC and DXS148, both assigned to Xp21, indicating that, contrary to previous linkage studies, there is evidence of an RP locus distal to DXS7. This suggests that X-linked retinitis pigmentosa is genetically heterogeneous, i.e., caused by mutations at different loci.

摘要

利用位于Xp上的DNA标记,对三个患有X连锁视网膜色素变性的大型多代家系进行了连锁分析。在视网膜色素变性基因座(RP2)与标记基因座DXS7之间发现了约10%的重组,DXS7定位于Xp11.3带,此前在几个独立家系中报道其与RP2紧密连锁。然而,在本文所描述的家系中,RP2与同样定位于Xp21的标记基因座OTC和DXS148显示紧密连锁且无重组,这表明与先前的连锁研究相反,有证据表明在DXS7远端存在一个RP基因座。这表明X连锁视网膜色素变性在遗传上是异质性的,即由不同基因座的突变引起。

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