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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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Published in: | Frontiers in genetics 2022, Vol.13, p.998898-998898 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Report |
Language: | English |
Online Access: | Get full text |
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ISSN: | 1664-8021 1664-8021 |
DOI: | 10.3389/fgene.2022.998898 |