Neurotrophin-3 rs1805149A>G variant in Hirschsprung disease: An investigative study

The <i>NTF3</i> rs1805149A>G variant does not appear to be associated with HSCR susceptibility in the studied southern Chinese cohort. Further studies with larger sample sizes and multi-gene analysis are warranted to better understand the genetic basis of HSCR.

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Publication Details

Journal
World Journal of Gastrointestinal Surgery
Published
2026-02-25
DOI
https://doi.org/10.4240/wjgs.v18.i2.114724
Primary Topic
Congenital gastrointestinal and neural anomalies
Type
article
Field-Weighted Citation Impact
0.00
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article

Neurotrophin-3 rs1805149A>G variant in Hirschsprung disease: An investigative study

Menglong Lan, Ji Zeng, Fei Liu, Xiao-Gang Xu et al.
World Journal of Gastrointestinal Surgery
Congenital gastrointestinal and neural anomalies
article

Neurotrophin-3 rs1805149A>G variant in Hirschsprung disease: An investigative study

Menglong Lan, Ji Zeng, Fei Liu, Xiao-Gang Xu, Yan-Qing Liu, Hui-Min Xia
article en

Abstract

The <i>NTF3</i> rs1805149A>G variant does not appear to be associated with HSCR susceptibility in the studied southern Chinese cohort. Further studies with larger sample sizes and multi-gene analysis are warranted to better understand the genetic basis of HSCR.

World Journal of Gastrointestinal SurgeryVol. 18(2)
Guangzhou Women and Children Medical Center (CN), Guangzhou Medical University (CN)
Openalex Percentile: Top 44%
Congenital gastrointestinal and neural anomalies
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