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NPHP1 gene deletion is a rare cause of Joubert sindrome related disorders

Authors :
Castori, M.
Valente, E. M.
Donati, M. A.
Salvi, S.
Fazzi, Elisa Maria
Procopio, E.
Galluccio, T.
Emma, F.
DALLA PICCOLA, B.
Bertini, E.
Publication Year :
2005
Publisher :
BMJ / British Medical Journal Publishing Group:PO Box 299, London WC1H 9TD United Kingdom:011 44 20 73836270, EMAIL: subscriptions@bmjgroup.com, INTERNET: http://www.bmjpg.com/bmj, Fax: 011 44 20 73836402, 2005.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.od......3662..6eb605e6966fe4b281a86358229d029b

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