Min Liang
Wenzhou Medical University(CN)First Affiliated Hospital of Wenzhou Medical University(CN)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, ATP Synthase and ATPases Research, Metabolism and Genetic Disorders, Vestibular and auditory disorders, Hemoglobinopathies and Related Disorders
Most-Cited Works
- → The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation(2015)103 cited
- → Leber’s hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation(2009)78 cited
- → Prevalence of MitochondrialND4Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy(2015)59 cited
- → MitochondrialND1Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy(2016)48 cited
- → Frequency and Spectrum of MitochondrialND6Mutations in 1218 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy(2014)46 cited
- → Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber’s hereditary optic neuropathy-associated mitochondrial DNA mutation(2016)42 cited