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

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Bibliographic Details
Main Authors:	Carolina Rojas, Maria Jose Hidalgo, Leticia Elgueta, Paula Segura, Erico Segovia, Luis Toro, Rosa Pardo, Gustavo Albornoz, Rosemarie Menke, Beatriz Urrutia, Miriam Alvo
Format:	Article
Language:	English
Published:	Elsevier 2024-04-01
Series:	Kidney International Reports
Online Access:	http://www.sciencedirect.com/science/article/pii/S2468024924008155
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