Autosomal dominant hypocalcemia in monozygotic twins caused by a de novo germline mutation near the amino-terminus of the human calcium receptor

Medicine & Life Sciences

• Familial Hypercalciuric Hypocalcemia 100%
• Calcium-Sensing Receptors 73%
• Germ-Line Mutation 62%
• Siblings 30%
• Hypocalcemia 19%
• Mutation 12%
• Twins 11%
• Missense Mutation 11%
• Droseraceae 10%
• Smart Materials 9%
• Molecular Biology 8%
• Parents 8%
• Automobiles 6%
• HEK293 Cells 5%
• Phosphatidylinositols 5%
• Aspartic Acid 5%
• Mutagenesis 5%
• Hydrolysis 5%
• Arginine 5%
• Salts 4%
• Complementary DNA 4%
• Genes 4%
• Peptides 3%
• Phenotype 3%
• In Vitro Techniques 2%
• Proteins 2%