Abstract
At present, even though we have accumulated a wealth of knowledge regarding structural, and molecular changes in ADPKD, the primary cause of the disease remains unknown. Obviously the gap in our understanding of the nature of the disease has been narrowed substantially over the past decade. With current techniques and efforts, the ultimate mystery of ADPKD should be resolved during the next decade.
Original language | English (US) |
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Pages (from-to) | 181-189 |
Number of pages | 9 |
Journal | Renal Failure |
Volume | 20 |
Issue number | 2 |
DOIs | |
State | Published - 1998 |
Funding
Ths work was supported by the Coleman Family Fund and by NM grant D28492.
Keywords
- Autosomal dominant
- Extracellular matrix
- Polycystic Kidney Disease
ASJC Scopus subject areas
- Critical Care and Intensive Care Medicine
- Nephrology