NOX5 is expressed aberrantly but not a critical pathogenetic gene in Hirschsprung disease

BACKGROUND: Hirschsprung disease (HSCR) is a congenital disorder characterized by the absence of intramural ganglion cells in the distal gastrointestinal tract (GI), which results in tonic contraction of the aganglionic gut segment and functional intestinal obstruction. Recent studies have suggested...

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Detalles Bibliográficos
Autores principales: Wang, Jing, Xiao, Jun, Meng, Xinyao, Chu, Xufeng, Zhuansun, Di Di, Xiong, Bo, Feng, Jiexiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008622/
https://www.ncbi.nlm.nih.gov/pubmed/33784990
http://dx.doi.org/10.1186/s12887-021-02611-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008622/
https://www.ncbi.nlm.nih.gov/pubmed/33784990
http://dx.doi.org/10.1186/s12887-021-02611-5

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