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Helen L, Paul W. Cystic disease and developmental kidney defects: Medullary Nephronophithisis-Medullary Cystic Kidney Disease Complex (NPH-MCKD). In: Heptinstall&apos;s Pathology of The Kidney. 6th ed. Charles J, Jean LO, Melvin MS, Fred GS, Eds. Lippincott Williams &amp; Wilkins, Phialdelphia, 2007: 1273-1278."},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Rohatgi R. Clinical manifestations of hereditary cystic kidney disease. Front Biosci 13: 4175-4197, 2008.","DOI":"10.2741\/2999"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Bisceglia M, Galliani CA, Senger C, et al. Renal cystic dseases:A review. Adv Anat Pathol 13: 26-56, 2006.","DOI":"10.1097\/01.pap.0000201831.77472.d3"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Wise SW, Hartman DS, Hardesty LA, et al. Renal medullary cystic disease: Assessment by MRI. Abdom Imaging 23: 649-651, 1998.","DOI":"10.1007\/s002619900423"},{"key":"5","unstructured":"5. Scolari F, Ghiggeri GM. Nephronophthisis-medullary cystic kidney disease: From bedside to bench and back again. Saudi J Kidney Dis Transpl 14: 316-327, 2003."},{"key":"6","doi-asserted-by":"publisher","unstructured":"6. Langner C, Ratschek M, Rehak P, Schips L, Zigeuner R. CD10 is a diagnostic and prognostic marker in renal malignancies. Histopathology 45: 460-467, 2004.","DOI":"10.1111\/j.1365-2559.2004.01982.x"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Yang XJ, Zhou M, Hes O, et al. Tubulocystic carcinoma of the kidney: Clinicopathologic and molecular characterization. Am J Surg Pathol 32: 177-187, 2008.","DOI":"10.1097\/PAS.0b013e318150df1d"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Hildebrandt F, Otto E, Rensing C, et al. Anovel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1. Net Genet 17: 149-153, 1997.","DOI":"10.1038\/ng1097-149"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Saunier S, Calado J, Heilig R, et al. 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A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution. Am J Hum Genet 71: 1161-1167, 2002.","DOI":"10.1086\/344395"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Otto EA, Loeys B, Khanna J, et al. Nephrocystin-5, a ciliry IQ domain protein, is mutated in Senior-Loken syndrome are interacts with RPGR and calmodulin. Nat Genet 37: 282-288, 2005.","DOI":"10.1038\/ng1520"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Sayer JA, Otto EA, O&apos;Toole JF, et al. The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nat Genet 38: 674-681, 2006.","DOI":"10.1038\/ng1786"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Attanasio M, Uhlenhaut NH, Sousa VH, et al. Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis. 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