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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 2 |
2011 | 1 |
2017 | 1 |
2024 | 0 |
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Functional analysis of pharmacogenetic variants of human organic cation/carnitine transporter 2 (hOCTN2) identified in Singaporean populations.
Biochem Pharmacol. 2011 Dec 1;82(11):1692-9. doi: 10.1016/j.bcp.2011.08.008. Epub 2011 Aug 16.
Biochem Pharmacol. 2011.
PMID: 21864509
Molecular spectrum of SLC22A5 (OCTN2) gene mutations detected in 143 subjects evaluated for systemic carnitine deficiency.
Li FY, El-Hattab AW, Bawle EV, Boles RG, Schmitt ES, Scaglia F, Wong LJ.
Li FY, et al.
Hum Mutat. 2010 Aug;31(8):E1632-51. doi: 10.1002/humu.21311.
Hum Mutat. 2010.
PMID: 20574985
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Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.
Neubauer J, Lecca MR, Russo G, Bartsch C, Medeiros-Domingo A, Berger W, Haas C.
Neubauer J, et al.
Eur J Hum Genet. 2017 Apr;25(4):404-409. doi: 10.1038/ejhg.2016.199. Epub 2017 Jan 11.
Eur J Hum Genet. 2017.
PMID: 28074886
Free PMC article.
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Genetic variations of the SLC22A5 gene in the Chinese and Indian populations of Singapore.
Toh DS, Yee JY, Koo SH, Murray M, Lee EJ.
Toh DS, et al.
Drug Metab Pharmacokinet. 2010;25(1):112-9. doi: 10.2133/dmpk.25.112.
Drug Metab Pharmacokinet. 2010.
PMID: 20208395
Free article.
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