A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Barbara Vona, Neda Mazaheri, Sheng‐Jia Lin, Lucy A Dunbar, Reza Maroofian, Héla Azaiez, Kevin T. Booth, Sandrine Vitry, Abolfazl Rad, Franz Rüschendorf,

Human Genetics · 2021 · 27 citations · 53 references

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