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Biparental Inheritance of Mitochondrial DNA in Humans.
Luo S, Valencia CA, Zhang J, Lee NC, Slone J, Gui B, Wang X, Li Z, Dell S, Brown J, Chen SM, Chien YH, Hwu WL, Fan PC, Wong LJ, Atwal PS, Huang T. Luo S, et al. Proc Natl Acad Sci U S A. 2018 Dec 18;115(51):13039-13044. doi: 10.1073/pnas.1810946115. Epub 2018 Nov 26. Proc Natl Acad Sci U S A. 2018. PMID: 30478036 Free PMC article.
Diagnosis of mitochondrial myopathies.
Milone M, Wong LJ. Milone M, et al. Mol Genet Metab. 2013 Sep-Oct;110(1-2):35-41. doi: 10.1016/j.ymgme.2013.07.007. Epub 2013 Jul 17. Mol Genet Metab. 2013. PMID: 23911206 Review.
Mitochondrial disorder with OPA1 mutation lacking optic atrophy.
Milone M, Younge BR, Wang J, Zhang S, Wong LJ. Milone M, et al. Mitochondrion. 2009 Jul;9(4):279-81. doi: 10.1016/j.mito.2009.03.001. Epub 2009 Mar 20. Mitochondrion. 2009. PMID: 19303950
Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B.
Shaibani A, Shchelochkov OA, Zhang S, Katsonis P, Lichtarge O, Wong LJ, Shinawi M. Shaibani A, et al. Arch Neurol. 2009 Aug;66(8):1028-32. doi: 10.1001/archneurol.2009.139. Arch Neurol. 2009. PMID: 19667227 Free PMC article.
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