Familial Esophageal Squamous Cell Carcinoma with damaging rare/germline mutations in KCNJ12/KCNJ18 and GPRIN2 genes-Reference-Cited by-同舟云学术

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Familial Esophageal Squamous Cell Carcinoma with damaging rare/germline mutations in KCNJ12/KCNJ18 and GPRIN2 genes

Published:2018-02 Issue: Volume:221 Page:46-52
ISSN:2210-7762
Container-title:Cancer Genetics
language:en
Short-container-title:Cancer Genetics

Author:

Khalilipour Narjes,Baranova Ancha,Jebelli Amir,Heravi-Moussavi Alireza,Bruskin Sergey,Abbaszadegan Mohammad Reza

Funder

Mashhad University of Medical Sciences

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference43 articles.

1. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012;Ferlay;Int J Cancer,2015

2. Epidemiology of esophageal cancer;Zhang;World J Gastroenterol,2013

3. Genetic landscape of esophageal squamous cell carcinoma;Gao;Nat Genet,2014

4. Five common cancers in Iran;Kolahdoozan;Arch Iran Med,2010

5. Germline BRCA2 mutations and the risk of esophageal squamous cell carcinoma;Akbari;Oncogene,2008

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