首页> 外文期刊>European journal of human genetics: EJHG >Parental origin of mutations in sporadic cases of Treacher Collins syndrome.
【24h】

Parental origin of mutations in sporadic cases of Treacher Collins syndrome.

机译:Treacher Collins综合征零星病例中父母的突变起源。

获取原文
获取原文并翻译 | 示例
           

摘要

In some autosomal dominant conditions, there is a correlation between new mutations and paternal age, with new mutations arising almost exclusively in the male germ line. To test this hypothesis in Treacher Collins syndrome, we analyzed 22 sporadic cases, determining the parental origin of the pathogenic mutation in 10 informative families. Mutations were found to be of both paternal and maternal origin, without a detectable parental age effect, confirming that a paternal age effect is not universal to all autosomal dominant disorders. A discussion on the parental origin of mutations and paternal age effect in other diseases is included.
机译:在某些常染色体显性遗传条件下,新突变与父本年龄之间存在相关性,新突变几乎只在雄性种系中出现。为了在Treacher Collins综合征中检验这一假设,我们分析了22例散发病例,确定了10个信息丰富的家庭的致病突变的父母起源。发现突变来自父亲和母亲,没有可检测到的父母年龄效应,这证实了父亲年龄效应并非对所有常染色体显性遗传性疾病都是普遍的。包括有关父母亲突变的起源和其他疾病中父母年龄效应的讨论。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号