Brain size reductions associated with endothelin B receptor mutation, a cause of Hirschsprung’s disease

BACKGROUND: ET(B) has been reported to regulate neurogenesis and vasoregulation in foetal development. Its dysfunction was known to cause HSCR, an aganglionic colonic disorder with syndromic forms reported to associate with both small heads and developmental delay. We therefore asked, "is CNS m...

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Bibliografiske detaljer
Udgivet i:BMC Neurosci
Main Authors: Chen, Ko-Chin, Song, Zan-Min, Croaker, Geoffrey D.
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2021
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8214790/
https://ncbi.nlm.nih.gov/pubmed/34147087
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12868-021-00646-z
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