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Article

Genetic alterations of δ-catenin/NPRAP/Neurojungin (CTNND2): functional implications in complex human diseases.

Human genetics - 1 Oct 2016

Lu Qun, Aguilar Byron J, Li Mingchuan, Jiang Yongguang, Chen Yan-Hua

Abstract excerpt

Some genes involved in complex human diseases are particularly vulnerable to genetic variations such as single nucleotide polymorphism, copy number variations, and mutations. For example, Ras mutations account for over 30 % of all human cancers. Additionally, there are some genes that can display different variations with functional impact in different diseases that are unrelated. One such gene stands out:...

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Identifiers

PMID: 27380241
DOI: 10.1007/s00439-016-1705-3
PMCID: PMC5021578

Genes

CTNND2

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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