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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1993 | 1 |
1998 | 2 |
1999 | 1 |
2004 | 1 |
2023 | 0 |
PubMed (OMIM) for id: 1648411
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Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome.
J Med Genet. 2004 Jan;41(1):14-7. doi: 10.1136/jmg.2003.014316.
J Med Genet. 2004.
PMID: 14729820
Free PMC article.
Human mitochondrial complex I in health and disease.
Smeitink J, van den Heuvel L.
Smeitink J, et al.
Am J Hum Genet. 1999 Jun;64(6):1505-10. doi: 10.1086/302432.
Am J Hum Genet. 1999.
PMID: 10330338
Free PMC article.
Review.
No abstract available.
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Intron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain.
Emahazion T, Beskow A, Gyllensten U, Brookes AJ.
Emahazion T, et al.
Cytogenet Cell Genet. 1998;82(1-2):115-9. doi: 10.1159/000015082.
Cytogenet Cell Genet. 1998.
PMID: 9763677
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cDNA sequence and chromosomal localization of the remaining three human nuclear encoded iron sulphur protein (IP) subunits of complex I: the human IP fraction is completed.
Loeffen J, van den Heuvel L, Smeets R, Triepels R, Sengers R, Trijbels F, Smeitink J.
Loeffen J, et al.
Biochem Biophys Res Commun. 1998 Jun 29;247(3):751-8. doi: 10.1006/bbrc.1998.8882.
Biochem Biophys Res Commun. 1998.
PMID: 9647766
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The gene locus of the proton-translocating NADH: ubiquinone oxidoreductase in Escherichia coli. Organization of the 14 genes and relationship between the derived proteins and subunits of mitochondrial complex I.
Weidner U, Geier S, Ptock A, Friedrich T, Leif H, Weiss H.
Weidner U, et al.
J Mol Biol. 1993 Sep 5;233(1):109-22. doi: 10.1006/jmbi.1993.1488.
J Mol Biol. 1993.
PMID: 7690854
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