Associated Papers
Clinical and molecular features of two diabetes families carrying mitochondrial ND1 T3394C mutation.
You X et al.
Irish Journal of Medical Science, 2022
Leber's Hereditary Optic Neuropathy: the roles of mitochondrial transfer RNA variants.
Ding Y et al.
Peerj, 2021
Mitochondrial tRNA mutations in 887 Chinese subjects with hearing loss.
Zheng J et al.
Mitochondrion, 2020
[The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families].
Zhou HH et al.
Yi Chuan = Hereditas, 2012
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