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

<div>Audiograms of some members participating in this study in the four Chinese families. Blue crosses and red circles represent the air conduction hearing threshold levels of left and right ears, respectively. Asterisks indicate the families with LOXHD1 mutations identified in this study. Gender and age are shown below the audiogram of each individual.</div>

BioMed Research International

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Figure 2

Figure 2: Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families 