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CHARCOT-MARIE-TOOTH SYNDROME AND GENETIC FOCAL SEGMENTAL GLOMERULOSCLEROSIS: DE NOVO MUTATION OF THE INF2 GENE
 
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E-Poster
https://storage.unitedwebnetwork.com/files/1099/e3cf10d690c6c526026832876f151980.pdf
Abstract Title
CHARCOT-MARIE-TOOTH SYNDROME AND GENETIC FOCAL SEGMENTAL GLOMERULOSCLEROSIS: DE NOVO MUTATION OF THE INF2 GENE
First Name *
Carolina
Last Name *
Rojas
Co-author 1
Maria Jose Hidalgo mhidalgo@hcuch.cl Hospital Clinico Universidad de Chile Nephrology Santiago
Co-author 2
Leticia Elgueta lelgueta@hcuch.cl Hospital Clinico Universidad de Chile Nephrology Santiago
Co-author 3
Paula Segura psegura@hcuch.cl Hospital Clinico Universidad de Chile Pathological Anatomy Santiago
Co-author 4
Erico Segovia esegovia@hcuch.cl Hospital Clinico Universidad de Chile Nephrology Santiago
Co-author 5
Luis Toro latoroc@hcuch.cl Hospital Clinico Universidad de Chile Nephrology Santiago
Co-author 6
Rosa Pardo rpardo@hcuch.cl Hospital Clinico Universidad de Chile Genetics Santiago
Co-author 7
Gustavo Albornoz galbornoz@hcuch.cl Hospital Clinico Universidad de Chile Genetics Santiago
Co-author 8
Rosemarie Menke rnenke@hcuch.cl Hospital Clinico Universidad de Chile Genetics Santiago
Co-author 9
Beatriz Urrutia burrutia@hcuch.cl Hospital Clinico Universidad de Chile Rheumatology Santiago
Co-author 10
Miriam Alvo malvo@hcuch.cl Hospital Clinico Universidad de Chile Nephrology Santiago
Co-author 11
Co-author 12
Co-author 13
Co-author 14
Co-author 15