MSH3: a confirmed predisposing gene for adenomatous polyposis.

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Title: MSH3: a confirmed predisposing gene for adenomatous polyposis.
Authors: Villy MC; Department of Genetics, Université Paris Cité, Institut Curie, Paris, France marie-charlotte.villy@curie.fr., Masliah-Planchon J; Department of Genetics, PSL University, Institut Curie, Paris, France., Schnitzler A; Department of Genetics, PSL University, Institut Curie, Paris, France., Delhomelle H; Department of Genetics, PSL University, Institut Curie, Paris, France., Buecher B; Department of Genetics, PSL University, Institut Curie, Paris, France., Filser M; Department of Genetics, PSL University, Institut Curie, Paris, France., Merchadou K; Clinical Bioinformatics Unit, Institut Curie, Paris, France., Golmard L; Department of Genetics, PSL University, Institut Curie, Paris, France., Melaabi S; Department of Genetics, PSL University, Institut Curie, Paris, France., Vacher S; Department of Genetics, PSL University, Institut Curie, Paris, France., Blanluet M; Department of Genetics, PSL University, Institut Curie, Paris, France., Suybeng V; Department of Genetics, PSL University, Institut Curie, Paris, France., Corsini C; Medical Genetics Department, Centre Hospitalier Regional Universitaire de Montpellier, Montpellier, France., Dhooge M; Oncogenetic Unit, Department of Gastroenterology, AP-HP Centre-Université de Paris, Hopital Cochin, Paris, France., Hamzaoui N; Department of Genetics, AP-HP Centre-Université de Paris, Hospital Cochin, Paris, France., Farelly S; Oncogenetic Unit, Department of Gastroenterology, AP-HP Centre-Université de Paris, Hopital Cochin, Paris, France., Ait Omar A; Department of Gastroenterology, Hôpital Avicenne, Bobigny, France., Benamouzig R; Department of Gastroenterology, Hôpital Avicenne, Bobigny, France., Caumette V; Department of Genetics, Hôpitaux Universitaires Henri Mondor, Creteil, France., Bahuau M; Department of Genetics, Hôpitaux Universitaires Henri Mondor, Creteil, France., Cucherousset J; Department of Pathology, GHI Le Raincy-Montfermeil, Montfermeil, France., Allory Y; Department of Pathology, Université Paris-Saclay, Institut Curie, Paris, France., Stoppa-Lyonnet D; Department of Genetics, Université Paris Cité, Institut Curie, Paris, France., Bieche I; Department of Genetics, Université Paris Cité, Institut Curie, Paris, France., Colas C; Department of Genetics, PSL University, Institut Curie, Paris, France.
Source: Journal of medical genetics [J Med Genet] 2023 Nov 27; Vol. 60 (12), pp. 1198-1205. Date of Electronic Publication: 2023 Nov 27.
Publication Type: Journal Article
Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1468-6244
DOI:10.1136/jmg-2023-109341