WCN24-2383 CHARCOT-MARIE-TOOTH SYNDROME AND GENETIC FOCAL SEGMENTAL GLOMERULOSCLEROSIS: DE NOVO MUTATION OF THE INF2 GENE - Carolina Rojas; Maria Jose Hidalgo; Leticia Elgueta; Paula Segura; Erico Segovia; Luis Toro; Rosa Pardo; Gustavo Albornoz; Rosemarie Menke; Beatriz Urrutia; Miriam Alvo (Kidney International Reports)