Novel MNX1 mutations and genotype–phenotype analysis of patients with Currarino syndrome | Orphanet Journal of Rare Diseases | Full Text

Novel MNX1 mutations and genotype–phenotype analysis of patients with Currarino syndrome | Orphanet Journal of Rare Diseases | Full Text

Novel MNX1 mutations and genotype–phenotype analysis of patients with Currarino syndrome

Currarino syndrome (CS) is a specific complex of congenital caudal anomalies, including anorectal malformations, presacral mass and sacral anomalies. Mutations in the MNX1 gene are closely related to CS and occur...

Authors:Lu Han, Zhen Zhang, Hui Wang, Hui Song, Qing Gao, Yuchun Yan, Ran Tao, Ping Xiao, Long Li, Qian Jiang and Qi Li

Citation:Orphanet Journal of Rare Diseases 2020 15:155

Content type:Research

 

Published on: 22 June 2020

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