A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome
Mitchell-Riley syndrome is a genetic disorder characterized by neonatal diabetes, pancreatic hypoplasia, intestinal atresia and/or malrotation, biliary atresia, and gallbladder aplasia or hypoplasia. It was considered a variant of the Martinez-Frias syndrome with similar phenotypic characteristics,...
| Main Authors: | , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Galenos Publishing
2016
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096485/ |