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