Found: 9
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Molecular characterization of two Chinese pedigrees with maternally inherited hypertension.
- Published in:
- Journal of Gene Medicine, 2021, v. 23, n. 4, p. 1, doi. 10.1002/jgm.3328
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- Article
Mitochondrial tRNA Gln 4394C>T Mutation May Contribute to the Clinical Expression of 1555A>G-Induced Deafness.
- Published in:
- Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101794
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- Article
Lesch-Nyhan Syndrome in a Chinese Family with Mutation in the Hypoxanthine-Guanine Phosphoribosyltransferase Gene.
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- Clinical Laboratory, 2018, v. 64, p. 197, doi. 10.7754/Clin.Lab.2017.170813
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- Article
Mitochondrial Diabetes is Associated with tRNA<sup>Leu(UUR)</sup> A3243G and ND6 T14502C Mutations.
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- Diabetes, Metabolic Syndrome & Obesity: Targets & Therapy, 2022, v. 15, p. 1687, doi. 10.2147/DMSO.S363978
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- Article
Suicide Risk Assessment in a Modern Asian Adolescent Community: A Cultural-relevant Perspective.
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- Asian Journal of Interdisciplinary Research (AJIR), 2023, v. 6, n. 3, p. 15, doi. 10.54392/ajir2333
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- Article
Leber's Hereditary Optic Neuropathy: the roles of mitochondrial transfer RNA variants.
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- PeerJ, 2021, p. 1, doi. 10.7717/peerj.10651
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- Article
Mitochondrial Diabetes Is Associated with the ND4 G11696A Mutation.
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- Biomolecules (2218-273X), 2023, v. 13, n. 6, p. 907, doi. 10.3390/biom13060907
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- Article
The Association Between Mitochondrial tRNA<sup>Glu</sup> Variants and Hearing Loss: A Case-Control Study.
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- Pharmacogenomics & Personalized Medicine, 2024, v. 17, p. 77, doi. 10.2147/PGPM.S441281
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- Article
Late onset of type 2 diabetes is associated with mitochondrial tRNA<sup>Trp</sup> A5514G and tRNA<sup>Ser(AGY)</sup> C12237T mutations.
- Published in:
- Journal of Clinical Laboratory Analysis, 2022, v. 36, n. 1, p. 1, doi. 10.1002/jcla.24102
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- Article