Upregulation of the Nr2f1-A830082K12Rik gene pair in murine neural crest cells results in a complex phenotype reminiscent of Waardenburg syndrome type 4
Waardenburg syndrome is a neurocristopathy characterized by a combination of skin and hair depigmentation, and inner ear defects. In the type 4 form, these defects show comorbidity with Hirschsprung disease, a disorder marked by an absence of neural ganglia in the distal colon, triggering functional...
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Main Authors: | Karl-F. Bergeron (Author), Chloé M. A. Nguyen (Author), Tatiana Cardinal (Author), Baptiste Charrier (Author), David W. Silversides (Author), Nicolas Pilon (Author) |
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Format: | Book |
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The Company of Biologists,
2016-11-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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