BRCA2 c.8827C>T pathogenic mutation in a consanguineous Chinese family with hereditary breast cancer-Reference-Cited by-同舟云学术

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BRCA2 c.8827C>T pathogenic mutation in a consanguineous Chinese family with hereditary breast cancer

Published:2020-07-20 Issue:9 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Wang Jiangfen¹,Qin Jiayue²^ORCID,Xi Chunfang¹,Zhang Yafen¹

Affiliation:

1. Department of General Surgery Shanxi Provincial People’s Hospital Taiyuan Shanxi China

2. Department of Medical Affairs Annoroad Gene Technology Co. Ltd Beijing China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1411

Reference24 articles.

1. Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence

2. Novel BRCA2 pathogenic variant c.5219 T > G; p.(Leu1740Ter) in a consanguineous Senegalese family with hereditary breast cancer

3. High prevalence of BRCA1 and BRCA2 mutations in unselected Nigerian breast cancer patients

4. Screening for BRCA1 and BRCA2 mutations among French-Canadian breast cancer cases attending an outpatient clinic in Montreal

5. The spectrum of BRCA mutations and characteristics of BRCA-associated breast cancers in China: Screening of 2,991 patients and 1,043 controls by next-generation sequencing

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