<?xml version='1.0' encoding='UTF-8'?><xml><records><record><source-app name="HighWire" version="7.x">Drupal-HighWire</source-app><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mosley, Mary</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Hildebrandt, Friedhelm</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Single-Gene Defects Elucidate Mechanisms of CKD</style></title><secondary-title><style face="normal" font="default" size="100%">MD Conference Express</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2015-01-01 00:00:00</style></date></pub-dates></dates><pages><style  face="normal" font="default" size="100%">6-7</style></pages><abstract><style  face="normal" font="default" size="100%">This article discusses single-gene (monogenic) mutations that cause steroid-resistant nephrotic syndrome, polycystic kidney disease, cystic kidney disease, early-onset chronic kidney disease, as well as new monogenic disease genes and pathogenic pathways.</style></abstract><number><style face="normal" font="default" size="100%">49</style></number><volume><style face="normal" font="default" size="100%">14</style></volume></record></records></xml>