{Reference Type}: Case Reports
{Title}: URAT1 mutations cause renal hypouricaemia combined with Fanconi syndrome in a Chinese patient.
{Author}: Du J;Jiang Y;Wang O;Li M;Xing XP;Xia W;
{Journal}: Nephrology (Carlton)
{Volume}: 23
{Issue}: 8
{Year}: Aug 2018
{Factor}: 2.358
{DOI}: 10.1111/nep.13190
{Abstract}: