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Wolfram syndrome: Phenotypic heterogeneity and novel genetic variants in the WFS1 gene
Síndrome de Wolfram: heterogeneidad fenotípica y nuevas variantes genéticas en el gen WFS1
Joana Lima Ferreiraa,
Corresponding author
joanalferreira@gmail.com

Corresponding author.
, Vanessa Carvalhob, Filipa Espadac, João Massanod,e, Ana Paula Marquesa, Rosa Maria Príncipea
a Department of Endocrinology, Hospital Pedro Hispano, Matosinhos Local Health Unit, Rua Dr. Eduardo Torres, 4464-513 Senhora da Hora, Matosinhos, Portugal
b Department of Neurology, Hospital Pedro Hispano, Matosinhos Local Health Unit, Rua Dr. Eduardo Torres, 4464-513 Senhora da Hora, Matosinhos, Portugal
c Department of Pediatrics, Hospital Pedro Hispano, Matosinhos Local Health Unit, Rua Dr. Eduardo Torres, 4464-513 Senhora da Hora, Matosinhos, Portugal
d Department of Neurology, Centro Hospitalar Universitário de São João, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Porto, Portugal
e Department of Clinical Neurosciences and Mental Health, Faculty of Medicine, University of Porto, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Porto, Portugal
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ISSN: 25300164
Original language: English
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