Article info

Download PDFPDF

NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders
  1. Correspondence to:
 Dr Enrico Bertini
 Molecular Medicine Unit, Department of Laboratory Medicine, Bambino Gesu’ Hospital IRCCS, Piazza S. Onofrio, 4, 00165 Rome, Italy; bertiniopbg.net
View Full Text

Citation

Castori M, Valente EM, Donati MA, et al
NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders

Publication history

  • Accepted October 31, 2004
  • Revised October 25, 2004
  • First published February 2, 2005.
Online issue publication 
February 02, 2005

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.