Brain size reductions associated with endothelin B receptor mutation, a cause of Hirschsprung's dise...
Brain size reductions associated with endothelin B receptor mutation, a cause of Hirschsprung's disease
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BioMed Central Ltd
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English
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BioMed Central Ltd
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ET.sub.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 maldevelopment a more general feature of ET.sub.B mutation?" To i...
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Full title
Brain size reductions associated with endothelin B receptor mutation, a cause of Hirschsprung's disease
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TN_cdi_gale_infotracmisc_A672256378
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A672256378
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ISSN
1471-2202
E-ISSN
1471-2202
DOI
10.1186/s12868-021-00646-z
