RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders
- F. Brancati
- , L. Travaglini
- , D. Zablocka
- , E. Boltshauser
- , P. Accorsi
- , G. Montagna
- , J. L. Silhavy
- , G. Barrano
- , E. Bertini
- , F. Emma
- , L. Rigoli
- , Richard Leventer
- , Padraic Grattan-Smith
- , Andreas Janecke
- , Marc D'Hooghe
- , Rudy Van Coster
- , Karin Dias
- , Carla Moco
- , Ana Moreira
- , Chong Ae Kim
Research output: Contribution to journal › Article › peer-review
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