Associated Papers
Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.
Dworschak GC et al.
Orphanet Journal of Rare Diseases, 2021
33836786 (PubMed )
Supplement: 13023_2021_1799_MOESM1_ESM.docx
Spectrum of MNX1 Pathogenic Variants and Associated Clinical Features in Korean Patients with Currarino Syndrome.
Lee S et al.
Annals of Laboratory Medicine, 2018
Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases.
Merello E et al.
European Journal of Medical Genetics, 2013
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