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Xiang-Dong Kong

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Open access Sep 2026

Long-read sequencing resolves complex CYP21A2 variants and identifies 2+0 carriers in 21-hydroxylase deficiency.

The complex CYP21A2 variants arising from high homology with its pseudogene CYP21A1P challenge the diagnosis of 21-hydroxylase deficiency (21-OHD). This study systematically evaluated long-read sequencing (LRS) for identifying complex structural variants of the CYP21A2 gene in 21-OHD in comparison with conventional mol...

Yan-Jie Xia, Di Cui, Dan-Hua Li et al. · 0 citations
Review Open access Aug 2026

Broadening horizons: Pathogenesis and therapeutics of renal ciliopathies

A review of renal ciliopathies systematically elucidates the molecular mechanisms and aberrant signaling pathways in renal ciliopathies, links genetic heterogeneity to clinical phenotypes, and lays a theoretical basis for prenatal diagnosis and novel therapies.

Qiaowei Zhang, S. Xue, Zhi Gao et al. · 0 citations

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