ZMIZ1-associated neurodevelopmental disorder and Hirschsprung disease
De novo mutations in the gene encoding transcription factor ZMIZ1, located on chromosome 10q22, were recently found to be associated with a novel neurodevelopmental syndrome [1]. In this case report we present a patient with developmental delay and Hirschsprung disease, who carries a de novo mutatio...
Main Authors: | Anders Valind, Pernilla Stenström, Sofie Samuelsson, Tord Jonson, Erik A. Eklund |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2021-08-01
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Series: | Journal of Pediatric Surgery Case Reports |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S221357662100110X |
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