A novel RBBP8(p.E281*) germline mutation is a predisposing mutation in familial hereditary cancer syndrome-Reference-Cited by-同舟云学术

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A novel RBBP8(p.E281*) germline mutation is a predisposing mutation in familial hereditary cancer syndrome

Published:2023-08-24 Issue:10 Volume:101 Page:1255-1265
ISSN:0946-2716
Container-title:Journal of Molecular Medicine
language:en
Short-container-title:J Mol Med

Author:

Yan Jinhua,Wu Jinzheng,Wang Yang,Di Xiaotang,Jiang Hao,Wen Doudou,Li Duo,Zhang Shubing^ORCID

Funder

the National Natural Science Foundation of China

the Natural Science Foundation of Hunan Province of China

The graduate student independent exploration and innovation project of Central South University

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Drug Discovery,Molecular Medicine

Link

https://link.springer.com/content/pdf/10.1007/s00109-023-02354-z.pdf

Reference46 articles.

1. Samadder NJ, Giridhar KV, Baffy N et al (2019) Hereditary cancer syndromes-a primer on diagnosis and management: part 1: breast-ovarian cancer syndromes. Mayo Clin Proc 94(6):1084–1098

2. Liu Q, Tan YQ (2019) Advances in identification of susceptibility gene defects of hereditary colorectal cancer. J Cancer 10(3):643–653

3. McKay GE, Zakas AL, Osman F et al (2021) Factors affecting genetic consultation in adolescent and young adult patients with sarcoma. J Natl Compr Canc Netw 1-8

4. Hereditary cancer syndromes and risk assessment (2019) ACOG committee opinion, Number 793. Obstet Gynecol 134(6):e143–e149

5. Futreal PA, Liu Q, Shattuck-Eidens D et al (1994) BRCA1 mutations in primary breast and ovarian carcinomas. Science 266(5182):120–122

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