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RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders
- Authors :
- Brancati, F
Travaglini, L
Zablocka, D
Boltshauser, E
Accorsi, P
Montagna, G
Silhavy, Jl
Barrano, G
Bertini, E
Emma, F
Rigoli, L
Dallapiccola, B
Gleeson, Jg
Valente, Em
- Publication Year :
- 2008
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.od......3983..f6665be1b56ac563e6264bd3f20bed46