MSH2 genomic deletions are a frequent cause of HNPCC.
作者： Juul Wijnen , Heleen van der Klift , Hans Vasen , P Meera Khan , Fred Menko
DOI: 10.1038/3795
关键词:
摘要: … Here, we report that genomic deletions at MSH2 also represent a frequent cause of HNPCC. In fact, these deletions comprise more than one-third of all pathogenic MSH2 mutations …
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