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bobin wang
(3 results)?
Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNAThr in eight Chinese pedigrees.
Mitochondrion. 2018 Sep;42:84-91. doi: 10.1016/j.mito.2017.12.003. Epub 2017 Dec 7.
Mitochondrion. 2018.
PMID: 29225014
A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function.
Zhou M, Xue L, Chen Y, Li H, He Q, Wang B, Meng F, Wang M, Guan MX.
Zhou M, et al. Among authors: wang b.
J Biol Chem. 2018 Jan 26;293(4):1425-1438. doi: 10.1074/jbc.RA117.000317. Epub 2017 Dec 8.
J Biol Chem. 2018.
PMID: 29222331
Free PMC article.
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