Article info
Electronic letters
NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders
- 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
Citation
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
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Copyright 2005 Journal of Medical Genetics