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CRISPR/Cas9-mediated Genomic Editing of Cluap1/IFT38 Reveals a New Role in Actin Arrangement.
Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1.
Compound heterozygous alterations in intraflagellar transport protein CLUAP1 in a child with a novel…
Overall Architecture of the Intraflagellar Transport (IFT)-B Complex Containing Cluap1/IFT38 as an E…
Functional Evaluation of Splicing for Variants of Uncertain Significance in Patients with Inherited …
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Study to Evaluate the Efficacy of Afatinib in Skull Base Chordoma
Multi-omics Study of Clinical Endpoints in CHD
A Study of Chinese Adults With Lymphoma
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase III Study of Fuzuloparib Combined …
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