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Li, V. GFM1 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5649 (accessed on 21 September 2026).
Li V. GFM1 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5649. Accessed September 21, 2026.
Li, Vivi. "GFM1 Gene" Encyclopedia, https://encyclopedia.pub/entry/5649 (accessed September 21, 2026).
Li, V. (2020, December 25). GFM1 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5649
Li, Vivi. "GFM1 Gene." Encyclopedia. Web. 25 December, 2020.
GFM1 Gene
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/gfm1

G elongation factor mitochondrial 1

genes

References

  1. Antonicka H, Sasarman F, Kennaway NG, Shoubridge EA. The molecular basis fortissue specificity of the oxidative phosphorylation deficiencies in patients withmutations in the mitochondrial translation factor EFG1. Hum Mol Genet. 2006 Jun1;15(11):1835-46.
  2. Balasubramaniam S, Choy YS, Talib A, Norsiah MD, van den Heuvel LP, Rodenburg RJ. Infantile Progressive Hepatoencephalomyopathy with Combined OXPHOS Deficiencydue to Mutations in the Mitochondrial Translation Elongation Factor Gene GFM1.JIMD Rep. 2012;5:113-22. doi: 10.1007/8904_2011_107.
  3. Coenen MJ, Antonicka H, Ugalde C, Sasarman F, Rossi R, Heister JG, Newbold RF,Trijbels FJ, van den Heuvel LP, Shoubridge EA, Smeitink JA. Mutant mitochondrial elongation factor G1 and combined oxidative phosphorylation deficiency. N Engl J Med. 2004 Nov 11;351(20):2080-6.
  4. Ravn K, Schönewolf-Greulich B, Hansen RM, Bohr AH, Duno M, Wibrand F,Ostergaard E. Neonatal mitochondrial hepatoencephalopathy caused by novel GFM1mutations. Mol Genet Metab Rep. 2015 Feb 20;3:5-10. doi:10.1016/j.ymgmr.2015.01.004.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Vivi Li
View Times: 1.0K
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 25 Dec 2020
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