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Li, V. GJC2 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5661 (accessed on 21 September 2026).
Li V. GJC2 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5661. Accessed September 21, 2026.
Li, Vivi. "GJC2 Gene" Encyclopedia, https://encyclopedia.pub/entry/5661 (accessed September 21, 2026).
Li, V. (2020, December 25). GJC2 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5661
Li, Vivi. "GJC2 Gene." Encyclopedia. Web. 25 December, 2020.
GJC2 Gene
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/gjc2

Gap junction protein gamma 2

genes

References

  1. Gotoh L, Inoue K, Helman G, Mora S, Maski K, Soul JS, Bloom M, Evans SH, Goto YI, Caldovic L, Hobson GM, Vanderver A. GJC2 promoter mutations causingPelizaeus-Merzbacher-like disease. Mol Genet Metab. 2014 Mar;111(3):393-398. doi:10.1016/j.ymgme.2013.12.001.Nov;119(3):293.
  2. Nahhas N, Conant A, Orthmann-Murphy J, Vanderver A, Hobson G.Pelizaeus-Merzbacher-Like Disease 1. 2017 Dec 21 [updated 2019 Jan 17]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle;1993-2020. Available from http://www.ncbi.nlm.nih.gov/books/NBK470716/
  3. Orthmann-Murphy JL, Freidin M, Fischer E, Scherer SS, Abrams CK. Two distinct heterotypic channels mediate gap junction coupling between astrocyte andoligodendrocyte connexins. J Neurosci. 2007 Dec 19;27(51):13949-57.
  4. Orthmann-Murphy JL, Salsano E, Abrams CK, Bizzi A, Uziel G, Freidin MM,Lamantea E, Zeviani M, Scherer SS, Pareyson D. Hereditary spastic paraplegia is anovel phenotype for GJA12/GJC2 mutations. Brain. 2009 Feb;132(Pt 2):426-38. doi: 10.1093/brain/awn328.
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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: 810
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 25 Dec 2020
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