Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1
Radboud University Nijmegen · Radboud University Medical Center · +4 more institutions
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Abstract
No abstract available for this paper.
Citation impact
815
total citations
- FWCI
- 23.66
- Percentile
- 100%
- References
- 25
Citations per year
Authors
18- MJMarjolijn J. L. LigtenbergCorresponding
Radboud University Nijmegen, Radboud University Medical Center
- RPRoland P. Kuiper
Radboud University Nijmegen, Radboud University Medical Center
- TLTsun Leung Chan
Queen Mary Hospital, Tung Wah Eastern Hospital, St. Paul's Co-educational College, University of Hong Kong
- MGMonique Goossens
Radboud University Nijmegen, Radboud University Medical Center
- KMKonnie M. Hebeda
Radboud University Nijmegen, Radboud University Medical Center
Topics & keywords
Topics
Keywords
- Biology
- MSH2
- Genetics
- Exon
- Germline mutation
- Germline
- Gene
- Lynch syndrome
UN Sustainable Development Goals
- Good health and well-being
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