Đang chuẩn bị liên kết để tải về tài liệu:
PDE1A polymorphism contributes to the susceptibility of nephrolithiasis

Không đóng trình duyệt đến khi xuất hiện nút TẢI XUỐNG Tải xuống

Previous studies have confirmed a family risk of nephrolithiasis (NL), but only 15% of all cases are associated with an identified monogenic factor. In clinical practice, our group encountered a patient with NL combined with cystic kidney disease that had 3 affected family members. No known mutations association with NL was detected in this family, and thus further investigation of the molecular cause of NL was deemed to be necessary. |