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                                       Details for article 240 of 1354 found articles
 
 
  WCN24-2383 CHARCOT-MARIE-TOOTH SYNDROME AND GENETIC FOCAL SEGMENTAL GLOMERULOSCLEROSIS: DE NOVO MUTATION OF THE INF2 GENE
 
 
Title: WCN24-2383 CHARCOT-MARIE-TOOTH SYNDROME AND GENETIC FOCAL SEGMENTAL GLOMERULOSCLEROSIS: DE NOVO MUTATION OF THE INF2 GENE
Author: Rojas, Carolina
Hidalgo, Maria Jose
Elgueta, Leticia
Segura, Paula
Segovia, Erico
Toro, Luis
Pardo, Rosa
Albornoz, Gustavo
Menke, Rosemarie
Urrutia, Beatriz
Alvo, Miriam
Appeared in: Kidney international reports
Paging: Volume 9 () nr. 4S pages S351
Year: 2024
Contents:
Publisher: Published by Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 240 of 1354 found articles
 
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