Analysis of the <i>RET</i>,<i>GDNF</i>, <i>EDN3</i>, and<i>EDNRB</i> genes in patients with intestinal neuronal dysplasia and Hirschsprung disease
BACKGROUND Hirschsprung disease (HSCR) is a frequent congenital disorder with an incidence of 1 in 5000 live births, characterised by the absence of parasympathetic intramural ganglion cells in the hindgut resulting in intestinal obstruction in neonates and severe constipation in infants and adults....
Gespeichert in:
| Hauptverfasser: | , , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Englisch |
| Veröffentlicht: |
2001
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| Online-Zugang: | https://doi.org/10.1136/gut.48.5.671 https://gut.bmj.com/content/gutjnl/48/5/671.full.pdf |
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