Homo sapiens gap junction protein, gamma 2, 47kDa, mRNA (cDNA clone MG - Nucleotide

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Mechanisms of Diseases Associated with Mutation in GJC2/Connexin 47. [Biomolecules. 2023]
Mechanisms of Diseases Associated with Mutation in GJC2/Connexin 47.
Abrams CK. Biomolecules. 2023 Apr 21; 13(4). Epub 2023 Apr 21.
Lack of embryonic homozygous or adult heterozygous lymphatic phenotypes for a Sos1 mutation and lack of lymphatic embryonic phenotypes for a homozygous Cx47 mutation in mice. [Lymphology. 2022]
Lack of embryonic homozygous or adult heterozygous lymphatic phenotypes for a Sos1 mutation and lack of lymphatic embryonic phenotypes for a homozygous Cx47 mutation in mice.
Geng X, Chen L, Srinivasan RS, Kylat RJ, Witte MH, Erickson RJ. Lymphology. 2022; 55(3):129-134.
Activation of the unfolded protein response by Connexin47 mutations associated with Pelizaeus-Merzbacher-like disease. [Mol Cell Neurosci. 2022]
Activation of the unfolded protein response by Connexin47 mutations associated with Pelizaeus-Merzbacher-like disease.
Flores-Obando RE, Freidin MM, Hernández AI, Abrams CK. Mol Cell Neurosci. 2022 May; 120:103716. Epub 2022 Mar 8.

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Nucleotide