“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, vol. 8, no. 9s, pp. 106–110, Nov. 2025, doi: 10.64149/J.Ver.8.9s.106-110.