Yếu tố khởi đầu dịch mã eIF-tiểu đơn vị 2B gamma (tiếng Anh: Translation initiation factor eIF-2B subunit gamma) là protein ở người được mã hóa bởi genEIF2B3.[2][3]
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van der Knaap MS, Leegwater PA, Könst AA, và đồng nghiệp (2002). “Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter”. Ann. Neurol. 51 (2): 264–70. doi:10.1002/ana.10112. PMID11835386.
Fogli A, Dionisi-Vici C, Deodato F, và đồng nghiệp (2003). “A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation”. Neurology. 59 (12): 1966–8. doi:10.1212/01.wnl.0000041666.76863.47. PMID12499492.
Ota T, Suzuki Y, Nishikawa T, và đồng nghiệp (2004). “Complete sequencing and characterization of 21,243 full-length human cDNAs”. Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID14702039.
Fogli A, Schiffmann R, Hugendubler L, và đồng nghiệp (2005). “Decreased guanine nucleotide exchange factor activity in eIF2B-mutated patients”. Eur. J. Hum. Genet. 12 (7): 561–6. doi:10.1038/sj.ejhg.5201189. PMID15054402.
Rual JF, Venkatesan K, Hao T, và đồng nghiệp (2005). “Towards a proteome-scale map of the human protein-protein interaction network”. Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID16189514.
Suragani RN, Kamindla R, Ehtesham NZ, Ramaiah KV (2006). “Interaction of recombinant human eIF2 subunits with eIF2B and eIF2alpha kinases”. Biochem. Biophys. Res. Commun. 338 (4): 1766–72. doi:10.1016/j.bbrc.2005.10.150. PMID16288713.
Mikami S, Masutani M, Sonenberg N, và đồng nghiệp (2006). “An efficient mammalian cell-free translation system supplemented with translation factors”. Protein Expr. Purif. 46 (2): 348–57. doi:10.1016/j.pep.2005.09.021. PMID16289705.