Associated Papers
Familial constipation and death: one family with Currarino syndrome.
Yang G et al.
Bmj Case Reports, 2025
Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases.
Merello E et al.
European Journal of Medical Genetics, 2013
MNX1 (HLXB9) mutations in Currarino patients.
Garcia-Barceló MM et al.
Journal of Pediatric Surgery, 2009
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