Publications
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[ Author] Title Year Filters: First Letter Of Last Name is R and Author is Roosing, Susanne [Clear All Filters]
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome. Elife 4, e06602 (2015).
Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes. J Med Genet 53, 608-15 (2016).