Neonatal diabetes and congenital malabsorptive diarrhea attributable to a novel mutation in the human neurogenin-3 gene coding sequence

Medicine & Life Sciences

• Diarrhea 98%
• Nonsense Codon 90%
• Mutation 66%
• Western Blotting 53%
• Chromogranin A 50%
• Neuroendocrine Cells 50%
• Genes 47%
• Pancreatic Elastase 46%
• Amylases 43%
• Proteins 43%
• Luciferases 36%
• Small Intestine 36%
• Transcriptional Activation 35%
• Gestational Age 34%
• Pancreas 33%
• Blood Glucose 32%
• Research Design 31%
• Amino Acids 27%
• Parturition 27%
• Biopsy 23%
• Growth 19%
• Serum 17%
• Child 17%

Chemical Compounds

• Mutation 100%
• Protein 48%
• Glucose 29%
• Acid 13%