Molecular effects of novel mutations in Hesx1/HESX1 associated with human pituitary disorders

Medicin og biovidenskab

• Amino Acid Substitution 12%
• Amino Acids 8%
• Cell Culture Techniques 8%
• Central Nervous System 8%
• Child 5%
• DNA 12%
• Homeobox Genes 13%
• Homeodomain Proteins 15%
• In Vitro Techniques 5%
• Missense Mutation 11%
• Mutation 38%
• Pedigree 12%
• Phenotype 27%
• Pituitary Diseases 100%
• Point Mutation 11%
• Population 9%
• Proteins 4%
• Septo-Optic Dysplasia 38%
• Vertebrates 10%