Polycystic Kidney, Autosomal Recessive
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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.