Publications
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Author Title [ Year
] Filters: Keyword is Ciliopathies and Author is Zhang, Wenjuan [Clear All Filters]
Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies. Hum Mutat 39, 152-166 (2018).
IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome. Hum Mol Genet 25, 4012-4020 (2016).
