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Polycystic Kidney, Autosomal Recessive
Subject Areas on Research
Another cystic mystery solved.
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.
Sec63 and Xbp1 regulate IRE1α activity and polycystic disease severity.
Transplantation and autosomal recessive polycystic kidney disease.
