| 1 | NDUFB8, NDUFB8D
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| NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals with Leigh-like Encephalomyopathy.
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| Piekutowska-Abramczuk D, Assouline Z, Mataković L, Feichtinger RG, Koňařiková E, Jurkiewicz E, Stawiński P, Gusic M, Koller A, Pollak A, Gasperowicz P, Trubicka J, Ciara E, Iwanicka-Pronicka K, Rokicki D, Hanein S, Wortmann SB, Sperl W, Rötig A, Prokisch H, Pronicka E, Płoski R, Barcia G, Mayr JA.
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| Am J Hum Genet 102(3):460-467. doi: 10.1016/j.ajhg.2018.01.008. Epub 2018 Feb 8.
2018
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| 2 | NDUFB8
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| Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.
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| Grünewald A, Rygiel KA, Hepplewhite PD, Morris CM, Picard M, Turnbull DM.
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| Ann Neurol 79(3):366-78. doi: 10.1002/ana.24571. Epub 2016 Jan 28.
2016
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| 3 | NDUFB8, PTEN
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| PTEN and NDUFB8 aberrations in cervical cancer tissue.
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| Hsieh SM, Maguire DJ, Lintell NA, McCabe M, Griffiths LR.
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| Adv Exp Med Biol 599:31-6.
2007
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| 4 | NDUFA1, NDUFA6, NDUFA7, NDUFB8, NDUFS8
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| Mapping of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping.
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| Emahazion T, et al.
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| Cytogenet Cell Genet 82 : 114. 1998
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| 5 | MT-ND1, MT-ND2, MT-ND3, MT-ND4L, MT-ND5, NDUFA10, NDUFA3, NDUFA7, NDUFA9, NDUFB10, NDUFB4, NDUFB5, NDUFB8, NDUFC2, NDUFS1, NDUFS7, NDUFS8, NDUFV2, NDUFV3
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| cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed.
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| Loeffen JL, et al.
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| Biochem Biophys Res Commun 253(2):415-22. 1998
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| 6 | NDUFA2, NDUFA6, NDUFA7, NDUFB8, NDUFS8
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| In situ hybridisation mapping of genomic clones for five human respiratory chain complex I genes.
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| Dunbar DR, Shibasaki Y, Dobbie L, Andersson B, Brookes AJ.
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| Cytogenet Cell Genet 78(1):21-4. 1997
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