| 1 | ADCK3, COQ2, COQ6, COQ9, PDSS1, PDSS2
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| Update on clinical aspects and treatment of selected vitamin-responsive disorders II (riboflavin and CoQ 10).
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| Horvath R.
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| J Inherit Metab Dis 35(4):679-87. doi: 10.1007/s10545-011-9434-1. Epub 2012 Jan 10. Review.
2012
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| 2 | COQ9, COQ9D
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| A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease.
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| Duncan AJ, Bitner-Glindzicz M, Meunier B, Costello H, Hargreaves IP, López LC, Hirano M, Quinzii CM, Sadowski MI, Hardy J, Singleton A, Clayton PT, Rahman S.
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| Am J Hum Genet 84(5):558-66. Epub 2009 Apr 16.
2009
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| 3 | COQ9
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| Coenzyme Q9 provides cardioprotection after converting into coenzyme Q10.
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| Lekli I, Das S, Das S, Mukherjee S, Bak I, Juhasz B, Bagchi D, Trimurtulu G, Krishnaraju AV, Sengupta K, Tosaki A, Das DK.
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| J Agric Food Chem 56(13):5331-7. Epub 2008 Jun 11.
2008
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| 4 | ABCC11, ABCC6P1, ABCC6P2, ACYP2, APOB48R, CCL22, CCP110, CDC37, CIAPIN1, CLN3, COQ9, CX3CL1, CXCR3, DDX28, DHX38, DOK4, EARS2, EARS2, EIF3CL, GDE1, GTF3C1, LKAP, MAZ, NOMO1, NOMO2, NPIPA1, NUPR1, ORIPL, PMFBP1, RBKH, SLC7A5P1, TCCK, UBFD1, XPO6, ZG16, ZP2
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| Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q.
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| Loftus BJ, Kim UJ, Sneddon VP, Kalush F, Brandon R, Fuhrmann J, Mason T,Crosby ML, Barnstead M, Cronin L, Deslattes Mays A, Cao Y, Xu RX, Kang HL,Mitchell S, Eichler EE, Harris PC, Venter JC, Adams MD.
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| Genomics 60(3):295-308. 1999
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