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Genitourinary manifestations of Lynch syndrome in the urological practice
OBJECTIVE: Lynch syndrome (LS) is an autosomal dominant hereditary disorder resulting from germline mutation in at least one of the four mismatch repair genes or in EPCAM gene. From a clinical perspective, LS patients exhibit an increased predisposition to multiple primary malignancies and early age...
Autores principales: | Lonati, Chiara, Simeone, Claudio, Suardi, Nazareno, Spiess, Philippe E., Necchi, Andrea, Moschini, Marco |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Second Military Medical University
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643301/ https://www.ncbi.nlm.nih.gov/pubmed/36381590 http://dx.doi.org/10.1016/j.ajur.2022.05.009 |
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