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Paper Details

Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes.
Orphanet Journal of Rare Diseases
3
2022
BAIAP2L2, CACNG1, CDH23, EYA1, GTPBP4, HKDC1, MYO15A, MYO6, OTOF, OTOG, PCNX2, PDZD7, PTPN11, SLC12A2, SOX10, STRC, SVEP1, TBC1D8, ZNF335, candidate genes, deafness, genes, genetic loci, hearing loss, hereditary hearing loss, non-syndromic or syndromic hearing loss, novel candidate genes, patients
Author NameAffiliation
Yoichiro KamataniRIKEN Center for Integrative Medical Sciences
Michiaki KuboRIKEN Center for Integrative Medical Sciences
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Release 1.2