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

Overview of attention for article published in Frontiers in Genetics, October 2022

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In the top 25% of all research outputs scored by Altmetric
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RT @CIBERER: 📅El diagnóstico genético de una paciente con el #síndromeWolfram-like permite mejorar su abordaje clínico https://t.co/ua7Zs9u…

RT @CIBERER: 📅El diagnóstico genético de una paciente con el #síndromeWolfram-like permite mejorar su abordaje clínico https://t.co/ua7Zs9u…

RT @CIBERER: 📅El diagnóstico genético de una paciente con el #síndromeWolfram-like permite mejorar su abordaje clínico https://t.co/ua7Zs9u…

RT @CIBERER: 📅El diagnóstico genético de una paciente con el #síndromeWolfram-like permite mejorar su abordaje clínico https://t.co/ua7Zs9u…

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