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Case report: De novo pathogenic variant in WFS1 causes Wolfram-like syndrome debuting with congenital bilateral deafness

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Bibliographic Details
Published in:Frontiers in genetics 2022, Vol.13, p.998898-998898
Main Authors: Alías, Laura, López de Heredia, Miguel, Luna, Sabina, Clivillé, Núria, González-Quereda, Lídia, Gallano, Pía, de Juan, Júlia, Pujol, Albert, Diez, Santiago, Boronat, Susana, Orús, César, Lasa, Adriana, Venegas, María Del Prado
Format: Report
Language:English
Online Access:Get full text
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ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2022.998898