Article info

PDF
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome
  1. Correspondence to:
 Dr Melissa A Parisi
 Division of Genetics and Developmental Medicine, Department of Pediatrics, University of Washington School of Medicine, Box 356320, 1959 NE Pacific St, Seattle, WA 98195, USA; mparisi{at}u.washington.edu
View Full Text

Citation

Parisi MA, Doherty D, Eckert ML, et al
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome

Publication history

  • Accepted August 25, 2005
  • Revised August 23, 2005
  • First published September 9, 2005.
Online issue publication 
March 31, 2006

Article Versions

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.