A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome
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* Corresponding author: Els van Riel E.vanRiel@umcutrecht.nl
Hereditary Cancer in Clinical Practice 2010, 8:7 doi:10.1186/1897-4287-8-7
Pre-publication versions of this article and reviewers' reports
| Original Submission - Version 1 | Manuscript | 07 May 2010 | |
| Reviewer's Report | Paivi Peltomaki | 04 Jun 2010 | |
| Reviewer's Report | hans morreau | 15 Jun 2010 | |
| Resubmission - Version 2 | Manuscript | Author's comment | 16 Jul 2010 |
| Editorial acceptance | 26 Jul 2010 | ||
| Published | 12 Aug 2010 |