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评估西班牙人群常染色体显性多囊肾病(ADPKD)中的基因座异质性。

Estimating locus heterogeneity in autosomal dominant polycystic kidney disease (ADPKD) in the Spanish population.

作者信息

Peral B, San Millán J L, Hernández C, Valero A, Lathrop G M, Beckmann J S, Moreno F

机构信息

Unidad de Genética Molecular, Hospital Ramón y Cajal, Madrid, Spain.

出版信息

J Med Genet. 1993 Nov;30(11):910-3. doi: 10.1136/jmg.30.11.910.

Abstract

Although most mutations causing ADPKD in European populations have been mapped to the PKD1 locus on chromosome 16, some of them appear to be unlinked to this locus. To evaluate the incidence of unlinked mutations in Spain we have typed 31 Spanish families from different geographical sites for six closely linked DNA polymorphic marker loci flanking PKD1 detected by probes D16S85, D16S21, D16S259, D16S125, D16S246, and D16S80. Multilocus linkage analysis indicated that in 26 families the disease resulted from PKD1 mutations, whereas in three families it resulted from mutations in a locus other than PKD1. The two other families were not informative. Using the HOMOG test, the incidence of the PKD1 linked mutations in Spain is 85%. Multipoint linkage analysis in the 26 PKD1 families showed that the disease locus lies in the interval between D16S259(pGGG1) and D16S125(26.6).

摘要

尽管在欧洲人群中,大多数导致常染色体显性多囊肾病(ADPKD)的突变已被定位到16号染色体上的PKD1基因座,但其中一些突变似乎与该基因座并无关联。为评估西班牙非连锁突变的发生率,我们利用探针D16S85、D16S21、D16S259、D16S125、D16S246和D16S80检测到的六个紧密连锁的DNA多态性标记基因座,对来自不同地理位置的31个西班牙家庭进行了基因分型。多位点连锁分析表明,在26个家庭中,疾病是由PKD1突变引起的,而在三个家庭中,疾病是由PKD1以外的基因座突变引起的。另外两个家庭无法提供有效信息。使用HOMOG检验,西班牙PKD1连锁突变的发生率为85%。对26个PKD1家庭进行的多点连锁分析表明,疾病基因座位于D16S259(pGGG1)和D16S125(26.6)之间的区间内。

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