A Novel Nonsense Mutation of<i>POU4F3</i>Gene Causes Autosomal Dominant Hearing Loss

Chi Zhang, Mingming Wang, Yun Xiao, +6

Neural Plasticity

Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay

Fengguo Zhang, Yun Xiao, Lei Xu, +6

BioMed Research International

Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family

Yalin Ma, Yun Xiao, Fengguo Zhang, +5

International Journal of Pediatric Otorhinolaryngology

Chinese FamilyDevelopmental BiologyMyo7a GeneGenetic DisorderGenetics +7

Three <i>MYO15A</i> Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss

Fengguo Zhang, Lei Xu, Yun Xiao, +3

Neural Plasticity

GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification +17

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

Xiaohui Bai, Chi Zhang, Fengguo Zhang, +4

BioMed Research International

<i>GJB2, SLC26A4</i>, and mitochondrial <i>DNA12S rRNA</i> hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China

Yalin Ma, Yun Xiao, Xiaohui Bai, +5

Acta Oto-Laryngologica

Glutathione Peroxidase 1 Protects Against Peroxynitrite-Induced Spiral Ganglion Neuron Damage Through Attenuating NF-κB Pathway Activation

Xue Wang, Yuechen Han, Fang Chen, +5

Frontiers in Cellular Neuroscience

Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome

Fengguo Zhang, Xiaohui Bai, Yun Xiao, +5

International Journal of Pediatric Otorhinolaryngology

Developmental AnomalyNovel MutationChinese FamilyDevelopmental BiologyMendelian Disorder +7

Prevalence of Mutations in Deafness‐Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China

Jianfen Luo, Xiaohui Bai, Fengguo Zhang, +7

Annals of Human Genetics

GeneticsGenetic EpidemiologyPathologyHearing HealthProfound Nshl +15

Cochlear Implantation in a Patient with a Novel <i>POU3F4</i> Mutation and Incomplete Partition Type-III Malformation

Xiuhua Chao, Yun Xiao, Fengguo Zhang, +5

Neural Plasticity