Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families

<div>Pedigrees of the hearing loss families and identified pathogenic variants. Black squares represent members with hearing loss. Genotypes are marked below each member. Arrow shows the proband. Asterisks indicate the families with LOXHD1 mutations identified in the present study.</div>

BioMed Research International

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Figure 1

Figure 1: Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families 