TY - GEN AU - Bröer,Stefan AU - Bailey,Charles G AU - Kowalczuk,Sonja AU - Ng,Cynthia AU - Vanslambrouck,Jessica M AU - Rodgers,Helen AU - Auray-Blais,Christiane AU - Cavanaugh,Juleen A AU - Bröer,Angelika AU - Rasko,John E J TI - Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters SN - 0021-9738 PY - 2008///1230 KW - Alleles KW - Amino Acid Transport Disorders, Inborn KW - genetics KW - Amino Acid Transport Systems, Neutral KW - Family KW - Female KW - Glycine Plasma Membrane Transport Proteins KW - Humans KW - Male KW - Mutation KW - Pedigree KW - Penetrance N1 - Publication Type: Journal Article; Research Support, Non-U.S. Gov't UR - https://doi.org/10.1172/JCI36625 ER -