“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” (2025) Vascular and Endovascular Review, 8(9s), pp. 106–110. doi:10.64149/J.Ver.8.9s.106-110.