Identification and Characterization of a Cryptic Genomic Deletion-Insertion in EYA1 Associated with Branchio-Otic Syndrome

von Zheng, Hao
Veröffentlicht in: Neural plasticity (2021)

Mutation in the Hair Cell Specific Gene POU4F3 Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans

von He, Longxia
Veröffentlicht in: Neural plasticity (2016)

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

von Chen, Penghui
Veröffentlicht in: Neural plasticity (2016)