Dong-mei Sun

发表

Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A variants may have a modifying role in the phenotypic manifestation of deafness‐associated 12S rRNA A1555G mutation in three Han Chinese pedigrees

Ronghua Li, Zhihua Tao, M. Guan, 2008, American journal of medical genetics. Part A.

Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.

Fangli Wu, J. Greinwald, Zhihua Tao, 2007, Gene.

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss.

Ronghua Li, M. Guan, L. Xue, 2010, Mitochondrion.

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.

Ronghua Li, Yaping Qian, Zhihua Tao, 2010, Mitochondrion.

GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss

Jing Zheng, Ye Chen, Min-Xin Guan, 2015, PloS one.

[Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation].

Li Yang, Jianxin Lu, Dong-mei Sun, 2008, Yi chuan = Hereditas.

Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.

Jiong Cai, Zhihua Tao, M. Guan, 2007, Biochemical and biophysical research communications.

[Hearing loss and epilepsy may be associated with the novel mitochondrial tRNASer(UCN) 7472delC mutation in a Chinese family].

M. Guan, Li Yang, Dong-mei Sun, 2009, Yi chuan = Hereditas.

Mutational spectrum of phenylketonuria in Jiangsu province

Yu Liang, Jia Song, Dong-mei Sun, 2015, European Journal of Pediatrics.

[Genetic analysis of family constellation for cochlear implant recipients].

M. Guan, Bobei Chen, Dong-mei Sun, 2009, Yi chuan = Hereditas.

The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.

Zhihua Tao, M. Guan, Li Yang, 2007, Biochemical and biophysical research communications.