NLRP3 Is Expressed in the Spiral Ganglion Neurons and Associated with Both Syndromic and Nonsyndromic Sensorineural Deafness

Figure 1

Pedigree of Family C277 with progressive hearing loss and MWS-related inflammatory symptoms. The genotype of the p.E313K mutation in NLRP3 was marked under the family members. Proband III3 was pointed by an arrow.