| Autor: |
Iglesias, D M, Telleria, D, Viribay, M, Herrera, M, Bernath, V A, Kornblihtt, A R, Martin, R S, Millán, J L |
| Zdroj: |
Nephrology Dialysis Transplantation; April 2000, Vol. 15 Issue: 4 p477-480, 4p |
| Abstrakt: |
Autosomal dominant polycystic kidney disease (ADPKD) is a genetically heterogeneous disorder that can be caused by mutations in at least three different genes. Several mutations have been identified in PKD1 and PKD2 genes. Most of the mutations found in PKD2 gene are predicted to cause premature termination of the protein. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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