ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.
Qian Zhou et al.PubMed ↗Full text ↗Publisher ↗
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