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A novel germline MLH1 mutation causing Lynch Syndrome in patients from the Republic of Macedonia
AIM: To implement molecular analysis in the clinical diagnosis and management of Lynch syndrome (LS). METHODS: We analyzed the mutations in MLH1 and MSH2 in the selected LS families from the Republic of Macedonia. RESULTS: We performed the very first genetic identification of LS families and charact...
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| Main Authors: | , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Croatian Medical Schools
2012
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3490460/ https://ncbi.nlm.nih.gov/pubmed/23100212 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3325/cmj.2012.53.496 |
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