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
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نتاج البحث: المساهمة في مجلة › Article › مراجعة النظراء
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