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A Mutation in the TRPC6 Cation Channel Causes Familial Focal Segmental Glomerulosclerosis

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Science  17 Jun 2005:
Vol. 308, Issue 5729, pp. 1801-1804
DOI: 10.1126/science.1106215

Article Information

vol. 308 no. 5729 1801-1804

PubMed: 
Print ISSN: 
Online ISSN: 
History: 
  • Received for publication October 8, 2004
  • Accepted for publication April 13, 2005
  • .

Article Versions

Author Information

  1. Michelle P. Winn1,2,*,
  2. Peter J. Conlon4,
  3. Kelvin L. Lynn5,
  4. Merry Kay Farrington1,2,
  5. Tony Creazzo3,
  6. April F. Hawkins1,
  7. Nikki Daskalakis1,2,
  8. Shu Ying Kwan2,
  9. Seth Ebersviller2,
  10. James L. Burchette5,
  11. Margaret A. Pericak-Vance1,2,
  12. David N. Howell5,
  13. Jeffery M. Vance1,2,*,
  14. Paul B. Rosenberg1,*
  1. 1 Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.
  2. 2 Center for Human Genetics, Duke University Medical Center, Durham, NC 27710, USA.
  3. 3 Department of Pediatrics, Duke University Medical Center, Durham, NC 27710, USA.
  4. 4 Department of Nephrology, Beaumont Hospital, Dublin, Ireland.
  5. 5 Department of Nephrology, Christchurch Hospital, Christchurch, New Zealand. 5Department of Pathology, Duke University Medical Center and Durham VA Medical Center, Durham, NC 27710, USA.
  1. * To whom correspondence should be addressed. E-mail: michelle.winn{at}duke.edu (M.P.W.); jeff{at}chg.duhs.duke.edu (J.M.V.); rosen029{at}mc.duke.edu (P.B.R.)

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