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Article

A Thr72Ala polymorphism in the NKG2D gene is associated with early symptomatic congenital cytomegalovirus disease.

Infection - 1 Jun 2015

Taniguchi Rumi, Koyano Shin, Suzutani Tatsuo, Goishi Keiji, Ito Yushi, Morioka Ichiro, Nakamura Hiroyuki, Yamada Hideto, Oka Akira, Inoue Naoki

Abstract excerpt

The potential risk factors for congenital cytomegalovirus (cCMV) infection or development of disease remain unclear. Here, we investigated the genetic polymorphisms in natural killer (NK) group 2, member D (NKG2D), an activating receptor expressed on NK cells, and in MHC class I-related chains A, the ligand of NKG2D, in 87 cCMV cases, and found that there was a significant association between cCMV disease and a...

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Source

Identifiers

PMID: 25861030
DOI: 10.1007/s15010-015-0774-x

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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