טוען...
Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation
Lynch syndrome (LS) is an autosomal dominant disorder characterized by an increased risk of extracolonic cancers and early age of onset. It is associated with germline mutations in the DNA mismatch repair (MMR) genes. We report a case of a patient with colorectal cancer referred to our medical genet...
שמור ב:
| הוצא לאור ב: | Turk J Gastroenterol |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Turkish Society of Gastroenterology
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6284679/ https://ncbi.nlm.nih.gov/pubmed/30289396 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/tjg.2018.17761 |
| תגים: |
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