| 1 | NDUFB3
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| Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.
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| Calvo SE, Compton AG, Hershman SG, Lim SC, Lieber DS, Tucker EJ, Laskowski A, Garone C, Liu S, Jaffe DB, Christodoulou J, Fletcher JM, Bruno DL, Goldblatt J, Dimauro S, Thorburn DR, Mootha VK.
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| Sci Transl Med 4(118):118ra10. doi: 10.1126/scitranslmed.3003310.
2012
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| 2 | NDUFB3, NDUFB3D
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| Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.
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| Haack TB, Haberberger B, Frisch EM, Wieland T, Iuso A, Gorza M, Strecker V, Graf E, Mayr JA, Herberg U, Hennermann JB, Klopstock T, Kuhn KA, Ahting U, Sperl W, Wilichowski E, Hoffmann GF, Tesarova M, Hansikova H, Zeman J, Plecko B, Zeviani M, Wittig I, Strom TM, Schuelke M, Freisinger P, Meitinger T, Prokisch H.
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| J Med Genet 49(4):277-83. doi: 10.1136/jmedgenet-2012-100846.
2012
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| 3 | ABI2, ALS2CR2, MAGI2, NDUFB3, NIF3L1, PSMA2L, TRAK2, TRAK2
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| Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2.
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| Hadano S, Yanagisawa Y, Skaug J, Fichter K, Nasir J, Martindale D, Koop BF, Scherer SW, Nicholson DW, Rouleau GA, Ikeda J, Hayden MR.
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| Genomics 71(2):200-13. 2001
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| 4 | NDUFB3, NDUFB3P1, NDUFB3P2, NDUFB3P3, NDUFB3P4, NDUFB3P5
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| Assignment of human NADH dehydrogenase (ubiquinone) 1 beta subcomplex 3 (NDUFB3) and of its four pseudogenes to human chromosomes 2q31.3, 1p13.3-->p13.1, 9q32-->q34.1, 14q22.3-->q23.1 and 14q32.2 by radiation hybrid mapping.
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| Jensen LL, Nielsen MM, Justesen J, Hansen LL.
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| Cytogenet Cell Genet 93(1-2):147-50. No abstract available. 2001
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| 5 | FAM109B,NDUFB3,NDUFC1
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| Identification and primary structure of five human NADH-ubiquinone oxidoreductase subunits.
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| Ton C, Hwang DM, Dempsey AA, Liew CC.
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| Biochem Biophys Res Commun 241(2):589-94. 1997
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