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Characterization of the c.793-1G > A splicing variant in CHEK2 gene as pathogenic: a case report
BACKGROUND: CHEK2 is involved in the DNA damage repair response Fanconi anemia (FA)-BRCA pathway. An increased risk for breast and other cancers has been documented in individuals who carry a single pathogenic CHEK2 variant. As for other genes involved in cancer predisposition, different types of pa...
Gorde:
| Argitaratua izan da: | BMC Med Genet |
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| Egile Nagusiak: | , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2019
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6660672/ https://ncbi.nlm.nih.gov/pubmed/31349801 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0862-3 |
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