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. Vascular and Endovascular Review, [S. l.], v. 8, n. 9s, p. 106–110, 2025. DOI: 10.64149/J.Ver.8.9s.106-110. Disponível em: https://verjournal.com/index.php/ver/article/view/726. Acesso em: 29 aug. 2026.