Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin-Reference-Cited by-同舟云学术

Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin

Published:2017-07-06 Issue:2 Volume:17 Page:179-185
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Krivokuca Ana,Dragos Vita Setrajcic,Stamatovic Ljiljana,Blatnik Ana,Boljevic Ivana,Stegel Vida,Rakobradovic Jelena,Skerl Petra,Jovandic Stevo,Krajc Mateja,Magic Mirjana Brankovic^ORCID,Novakovic Srdjan^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Link

http://link.springer.com/article/10.1007/s10689-017-0022-x/fulltext.html

Reference32 articles.

1. Walsh T, Casadei S, Lee MK et al (2011) Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. Proc Natl Acad Sci. doi: 10.1073/pnas.1115052108

2. Stegel V, Krajc M, Žgajnar J et al (2011) The occurrence of germline BRCA1 and BRCA2sequence alterations in Slovenian population. BMC Med Genet 12:9. doi: 10.1186/1471-2350-12-9

3. Novaković S, Milatović M, Cerkovnik P et al (2012) Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families. Int J Oncol 41:1619–1627. doi: 10.3892/ijo.2012.1595

4. Krajc M, Teugels E, Zgajnar J et al (2008) Five recurrent BRCA1/2 mutations are responsible for cancer predisposition in the majority of Slovenian breast cancer families. BMC Med Genet 9:83. doi: 10.1186/1471-2350-9-83

5. Krajc M, Zadnik V, Novaković S et al (2014) Geographical distribution of Slovenian BRCA1/2 families according to family origin: implications for genetic screening. Clin Genet 85:59–63. doi: 10.1111/cge.12119

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