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Article

Mutations in Fanconi anemia genes and the risk of esophageal cancer.

Human genetics - 1 May 2011

Akbari Mohammad R, Malekzadeh Reza, Lepage Pierre, Roquis David, Sadjadi Ali R, Aghcheli Karim, Yazdanbod Abbas, Shakeri Ramin, Bashiri Jafar, Sotoudeh Masoud, Pourshams Akram, Ghadirian Parviz, Narod Steven A

Abstract excerpt

The incidence of esophageal squamous cell carcinoma (ESCC) is very high in northeastern Iran. Previously, we reported a strong familial component of ESCC among Turkmens, who constitute approximately one-half of the population of this region. We hypothesized that the genes which cause Fanconi anemia might be candidate genes for ESCC. We sequenced the entire coding regions of 12 Fanconi anemia genes in the germline...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Fanconi Anemia Complementation Group D2 Protein

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Source

Identifiers

PMID: 21279724
DOI: 10.1007/s00439-011-0951-7

Genes

BRCA2
FANCA
FANCD2
FANCE
FANCL

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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