Associated Papers
Proactive functional classification of all possible missense single-nucleotide variants in KCNQ4.
Zheng H et al.
Genome Research, 2022
35760561 (PubMed )
Supplement: supp_gr.276562.122_Supplemental_Dataset.xlsx › Supplemental_Dataset_A
Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss.
Talebizadeh Z et al.
Human Mutation, 1999
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