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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8214790/ https://www.ncbi.nlm.nih.gov/pubmed/34147087 http://dx.doi.org/10.1186/s12868-021-00646-z |