A BRCA1 Splice Site Variant Responsible for Familial Ovarian Cancer in a Han-Chinese Family
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Biochemistry
Link
https://link.springer.com/content/pdf/10.1007/s11596-022-2527-2.pdf
Reference50 articles.
1. Toss A, Tomasello C, Razzaboni E, et al. Hereditary ovarian cancer: not only BRCA 1 and 2 genes. Biomed Res Int, 2015,2015:341723
2. Mansha M, Gill A, Thomson PC. Potential risk factors of ovarian cancer and analysis of CA125, a biomarker used for its monitoring and diagnosis. Mol Biol Rep, 2019,46(3):3325–3332
3. Roett MA, Evans P. Ovarian cancer: an overview. Am Fam Physician, 2009,80(6):609–616
4. Rojas V, Hirshfield KM, Ganesan S, et al. Molecular characterization of epithelial ovarian cancer: implications for diagnosis and treatment. Int J Mol Sci, 2016,17(12): 2113
5. Neff RT, Senter L, Salani R. BRCA mutation in ovarian cancer: testing, implications and treatment considerations. Ther Adv Med Oncol, 2017,9(8):519–531
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