Citations for
1COX6B1, COX6B1D
Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase.
Massa V, Fernandez-Vizarra E, Alshahwan S, Bakhsh E, Goffrini P, Ferrero I, Mereghetti P, D'Adamo P, Gasparini P, Zeviani M.
Am J Hum Genet 82(6):1281-9. Epub 2008 May 22. 2008
2AKT2, COX6B1, DAPK3, ETV2, KHSRP, OR7A10, OR7A5, OR7D2, OR7E24, S1PR5, ZNF607, ZNF610, ZSCAN5C
The DNA sequence and biology of human chromosome 19.
Grimwood J, and al.
Nature 428(6982):529-35. 2004
3COX6B1, COX7C
Amino acid replacement is rapid in primates for the mature polypeptides of COX subunits, but not for their targeting presequences.
Schmidt TR, Goodman M, Grossman LI.
Gene 286(1):13-9. 2002
4COX6B1
Assignment of the gene coding for human cytochrome c oxidase subunit VIbto chromosome 19, band q13.1. by fluorescence in situ hybridisation.
Taanman JW, et al.
Hum Genet 87 : 325-327. 1991
5COX6B1, COX6B1P3, COX6BP1, COX6BP2, COX6BP4
Human cytochrome c oxidase subunit VIB : characterization and mapping of a multigene family.
Carrero-Valenzuela RQ, et al.
Gene 102 : 229-236. 1991
6COX6B1
Isolation of cDNAs encoding subunit VIb of cytochrome c oxidase and steady-state levels of coxVIb mRNA in different tissues.
Taanman JW, Schrage C, Ponne NJ, Das AT, Bolhuis PA, de Vries H, Agsteribbe E.
Gene 93(2):285-91. 1990