TY - GEN AU - Bichet,D G AU - Turner,M AU - Morin,D TI - Vasopressin receptor mutations causing nephrogenic diabetes insipidus SN - 1081-650X PY - 1999///0115 KW - Amino Acid Sequence KW - Diabetes Insipidus, Nephrogenic KW - diagnosis KW - Heterozygote KW - Humans KW - Molecular Sequence Data KW - Mutation KW - Prenatal Diagnosis KW - Receptors, Vasopressin KW - genetics N1 - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review ER -