Komrower lecture: Inborn errors of signal transduction: Mutations in G proteins and G protein-coupled receptors as a cause of disease

Medicine & Life Sciences

• Albright's hereditary osteodystrophy 33%
• G-Protein-Coupled Receptors 100%
• Gain of Function Mutation 26%
• GTP-Binding Proteins 99%
• Loss of Function Mutation 22%
• Mutation 55%
• Nephrogenic Diabetes Insipidus 30%
• Neurotransmitter Agents 17%
• Peptide Hormones 23%
• Polyostotic Fibrous Dysplasia 30%
• Precocious Puberty 26%
• Protein Subunits 22%
• Signal Transduction 77%
• Therapeutics 3%