Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Type 28 of genetic inflammatory bowel disease is an autosomal recessive disorder caused by mutations of the IL10RB gene which codes a component of the IL10 receptor.
Inflammatory bowel disease
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Crohn disease-associated growth failure
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Inflammatory bowel disease 13
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Inflammatory bowel disease 25
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Inflammatory bowel disease 28
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IL10RA
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SEL1L
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| 1. |
Glocker EO et. al. (2009) Inflammatory bowel disease and mutations affecting the interleukin-10 receptor. 
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| 2. |
Begue B et. al. (2011) Defective IL10 signaling defining a subgroup of patients with inflammatory bowel disease.
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| 3. |
Mao H et. al. (2012) Exome sequencing identifies novel compound heterozygous mutations of IL-10 receptor 1 in neonatal-onset Crohn's disease.
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