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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes

Fig. 1

Frequencies of identified candidate genes associated with hearing loss in this study. Numbers in parenthesis indicate families carrying a candidate gene. Genes in red indicate those consistent with an autosomal recessive (AR) inheritance mode, and those in blue indicate genes consistent with an autosomal dominant (AD) inheritance mode. Sharp symbols (#) indicate that two deafness genes were found in different members of one family

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