Publications
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Filters: Author is Taylor, S Paige and Keyword is Cytoplasmic Dyneins [Clear All Filters]
Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome. Nat Commun 6, 7092 (2015).
Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies. Hum Mutat 39, 152-166 (2018).