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    WCN24-2383 CHARCOT-MARIE-TOOTH SYNDROME AND GENETIC FOCAL SEGMENTAL GLOMERULOSCLEROSIS: DE NOVO MUTATION OF THE INF2 GENE

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

    Published 2024-04-01
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