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Novel MSH2 splice-site mutation in a young patient with Lynch syndrome
Lynch Syndrome (LS) is associated with germline mutations in one of the mismatch repair (MMR) genes, including MutL homolog 1 (MLH1), MutS homolog 2 (MSH2), MSH6, PMS1 homolog 2, mismatch repair system component (PMS2), MLH3 and MSH3. The mutations identified in MMR genes are point mutations or larg...
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| Publicado no: | Mol Med Rep |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5928652/ https://ncbi.nlm.nih.gov/pubmed/29568967 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2018.8752 |
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