Osteogenesis imperfecta: Type I collagen and skeletal formation

Medicine & Life Sciences

• Osteogenesis Imperfecta 100%
• Collagen Type I 75%
• Mutation 16%
• Osteoblasts 14%
• Phenotype 13%
• Type IV Osteogenesis Imperfecta 13%
• Collagen 11%
• Endocrinologists 9%
• Joint Instability 9%
• Sclera 9%
• Bone and Bones 8%
• Loss of Function Mutation 8%
• Proteoglycans 8%
• Tendons 7%
• Genetic Therapy 6%
• Inborn Genetic Diseases 6%
• Osteoporosis 6%
• Extracellular Matrix 6%
• Molecular Biology 6%
• Differential Diagnosis 5%
• Fibroblasts 5%
• Proteins 5%
• Alleles 5%
• Technology 4%
• Skin 4%
• Growth 3%
• Child 3%
• Genes 3%