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PubMed (OMIM) for id: 4704
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NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect.
Clin Genet. 2018 Jan;93(1):111-118. doi: 10.1111/cge.13089. Epub 2017 Nov 21.
Clin Genet. 2018.
PMID: 28671271
Defective NDUFA9 as a novel cause of neonatally fatal complex I disease.
van den Bosch BJ, Gerards M, Sluiter W, Stegmann AP, Jongen EL, Hellebrekers DM, Oegema R, Lambrichs EH, Prokisch H, Danhauser K, Schoonderwoerd K, de Coo IF, Smeets HJ.
van den Bosch BJ, et al.
J Med Genet. 2012 Jan;49(1):10-5. doi: 10.1136/jmedgenet-2011-100466. Epub 2011 Nov 23.
J Med Genet. 2012.
PMID: 22114105
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Construction and evaluation of a hncDNA library of human 12p transcribed sequences derived from a somatic cell hybrid.
Baens M, Chaffanet M, Cassiman JJ, van den Berghe H, Marynen P.
Baens M, et al.
Genomics. 1993 Apr;16(1):214-8. doi: 10.1006/geno.1993.1161.
Genomics. 1993.
PMID: 8486360
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NADH:ubiquinone oxidoreductase from bovine heart mitochondria. cDNA sequences of the import precursors of the nuclear-encoded 39 kDa and 42 kDa subunits.
Fearnley IM, Finel M, Skehel JM, Walker JE.
Fearnley IM, et al.
Biochem J. 1991 Sep 15;278 ( Pt 3)(Pt 3):821-9. doi: 10.1042/bj2780821.
Biochem J. 1991.
PMID: 1832859
Free PMC article.
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