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A Rare Genetic Variant in SLC2A2 c.682 C > T (p.Arg228Ter) Underlying Complex Tubular Dysfunction and Progressive Bone Disease in Fanconi–Bickel Syndrome: A Novel Mutation with Systemic Implications. VER [Internet]. 2025 Nov. 14 [cited 2026 Aug. 29];8(9s):106-10. Available from: https://verjournal.com/index.php/ver/article/view/726