Mowat-Wilson syndrome associated with Hirschsprung disease
Purpose: Mowat-Wilson syndrome (MWS) is a rare autosomal dominant genetic disease caused by mutations in the zinc finger E-box binding homeobox 2 (ZEB2) gene. The syndrome is associated with Hirschsprung disease (HSCR). To investigate and report the clinical characteristics of MWS associated with HS...
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Elsevier,
2022-10-01T00:00:00Z.
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A1234.567 |
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| Nide 1 | Saatavissa |