Yuhua Zhu

发表

Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64.

Wei Li, X. Liu, K. Wrzeszczynski, 2011, American journal of human genetics.

Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family

Xuegong Zhang, P. Sham, J. Chen, 2014, Annals of human genetics.

Correlation analysis of phenotype and genotype of GJB2 in patients with non-syndromic hearing loss in China.

Yongyi Yuan, Shasha Huang, P. Dai, 2015, Gene.

Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China

J. Chen, X. Liu, D. Yan, 2011, Journal of Human Genetics.

Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation

Guo-jian Wang, Yongyi Yuan, Shasha Huang, 2014, BMC Genetics.

Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation.

P. Dai, Huijun Yuan, Dongyi Han, 2009, Mitochondrion.

A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss

Wenxue Tang, Xue Gao, Yue-shuai Song, 2014, PloS one.

Mutations in the mitochondrial 12S rRNA gene in elderly Chinese people

D. Kang, P. Dai, Huijun Yuan, 2015, Acta oto-laryngologica.

Discovery of sensorineural hearing loss and ossicle deformity in a Chinese Li nationality family with spondyloepiphyseal dysplasia congenita caused by p.G504S mutation of COL2A1

Z. Hou, Yuhua Zhu, Xiaocheng Wang, 2021, BMC Medical Genomics.

Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64.

Wei Li, X. Liu, K. Wrzeszczynski, 2011, American journal of human genetics.