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Dive into the research topics of 'CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders'. Together they form a unique fingerprint.- Sort by
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Francesco Brancati, Giuseppe Barrano, Jennifer L. Silhavy, Sarah E. Marsh, Lorena Travaglini, Stephanie L. Bielas, Maria Amorini, Dominika Zablocka, Hulya Kayserili, Lihadh Al-Gazali, Enrico Bertini, Eugen Boltshauser, Marc D'Hooghe, Elisa Fazzi, Elif Y. Fenerci, Raoul C.M. Hennekam, Andrea Kiss, Melissa M. Lees, Elysa Marco, Shubha R. Phadke
Research output: Contribution to journal › Article › peer-review