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Year | Number of Results |
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PubMed (OMIM) for id: 4715
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Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9.
J Med Genet. 2012 Feb;49(2):83-9. doi: 10.1136/jmedgenet-2011-100577. Epub 2011 Dec 26.
J Med Genet. 2012.
PMID: 22200994
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.
Item in Clipboard
Human NDUFB9 gene: genomic organization and a possible candidate gene associated with deafness disorder mapped to chromosome 8q13.
Lin X, Wells DE, Kimberling WJ, Kumar S.
Lin X, et al.
Hum Hered. 1999 Mar;49(2):75-80. doi: 10.1159/000022848.
Hum Hered. 1999.
PMID: 10077726
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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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The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-oto-renal syndrome.
Gu JZ, Lin X, Wells DE.
Gu JZ, et al.
Genomics. 1996 Jul 1;35(1):6-10. doi: 10.1006/geno.1996.0316.
Genomics. 1996.
PMID: 8661098
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