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范可尼贫血基因。

The Fanconi anemia genes.

作者信息

Carreau M, Buchwald M

机构信息

Department of Genetics, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Curr Opin Pediatr. 1998 Feb;10(1):65-9. doi: 10.1097/00008480-199802000-00013.

Abstract

Until recently, it had been thought that Fanconi anemia patients were distributed into five complementation groups. However, evidence now points to the existence of three new complementation groups, making the genetic basis of the disease more complicated than anticipated. Also, during the past year, the cloning of a second Fanconi anemia gene by both functional complementation and positional cloning has accelerated research of this disease. Although two genes of the eight characterized complementation groups have now been cloned, the function of their gene products still needs to be identified.

摘要

直到最近,人们一直认为范可尼贫血患者被分为五个互补组。然而,现在有证据表明存在三个新的互补组,这使得该疾病的遗传基础比预期的更加复杂。此外,在过去的一年里,通过功能互补和定位克隆对第二个范可尼贫血基因的克隆加速了对这种疾病的研究。尽管目前已克隆出八个已鉴定互补组中的两个基因,但其基因产物的功能仍有待确定。

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