MSH2基因缺失是遗传性非息肉病性结直肠癌（HNPCC）的常见病因。 - Suppr

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超能文献

MSH2 genomic deletions are a frequent cause of HNPCC.

作者信息

Wijnen J, van der Klift H, Vasen H, Khan P M, Menko F, Tops C, Meijers Heijboer H, Lindhout D, Møller P, Fodde R

出版信息

Nat Genet. 1998 Dec;20(4):326-8. doi: 10.1038/3795.

DOI:10.1038/3795

PMID:9843200

Abstract

摘要

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MSH2 genomic deletions are a frequent cause of HNPCC.MSH2基因缺失是遗传性非息肉病性结直肠癌（HNPCC）的常见病因。

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