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冯·希佩尔-林道病的基因型-表型相关性

Genotype-phenotype correlations in von Hippel-Lindau disease.

作者信息

Neumann H P, Bender B U

机构信息

Department of Nephrology and Hypertension, University of Freiburg, Germany.

出版信息

J Intern Med. 1998 Jun;243(6):541-5. doi: 10.1046/j.1365-2796.1998.00336.x.

Abstract

A total of 146 intragenic germline mutations of the von Hippel-Lindau (VHL) gene are known and this figure is still increasing. To date, information for mutation-specific genetic counselling is insufficient, since either the total number of carriers is very low or clinical information and investigation of symptomatic and asymptomatic is incomplete. This review summarizes all known mutations and includes the centres which performed the mutation analyses and may provide further information regarding specific mutations.

摘要

已知共有146种冯·希佩尔-林道(VHL)基因的基因内种系突变,且这一数字仍在增加。迄今为止,针对特定突变的遗传咨询信息不足,原因要么是携带者总数非常少,要么是对有症状和无症状者的临床信息及调查不完整。本综述总结了所有已知突变,并列出了进行突变分析的中心,这些中心可能会提供有关特定突变的更多信息。

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