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June 10, 2024

[Clinical characteristics and genetic analysis of four children with Rotor syndrome].

Yanfang Tan Wenxian Ouyang Tao Jiang Lian Tang Zhang Hui Ying Yu Xiaomei Qin Shuangjie Li

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Abstract

To explore the characteristics of SLCO1B1/SLCO1B3 gene variants among children with Rotor syndrome (RS).

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Cite This Study

Tan et al. (2024) studied this question.

synapsesocial.com/papers/68e65761b6db6435875e5d53 https://doi.org/10.3760/cma.j.cn511374-20220520-00342

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Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Recurrent SLCO1B1 and SLCO1B3 mutations identified in three patients with Rotor syndrome2025 · 1 citations
2A pedigree analysis of Rotor hyperbilirubinemia combined with hepatitis B virus infection in a SLCO1B1 and SLCO1B3 gene mutations patient2024
3Comprehensive analysis of RS1 gene mutations and clinical manifestations in nine unrelated X-linked retinoschisis (XLRS) Chinese familiesOriginal Research · 2026
4Exploring Roberts syndrome, unique manifestations in a four-month-old infant and genetic findings: A case report2025 · 1 citations
5Clinical characterization and molecular analysis of X-linked juvenile retinoschisis in a northern Chinese cohortOriginal Research · 2026

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