Human NCKX6 (pcDNA3.1+) Citations (1)
Originally described in: Molecular cloning of a sixth member of the K+-dependent Na+/Ca2+ exchanger gene family, NCKX6.Cai X, Lytton J J Biol Chem. 2004 Feb 13;279(7):5867-76. Epub 2003 Nov 18. PubMed Journal
Articles Citing Human NCKX6 (pcDNA3.1+)
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Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation. Stavsky A, Stoler O, Kostic M, Katoshevsky T, Assali EA, Savic I, Amitai Y, Prokisch H, Leiz S, Daumer-Haas C, Fleidervish I, Perocchi F, Gitler D, Sekler I. Commun Biol. 2021 Jun 2;4(1):666. doi: 10.1038/s42003-021-02114-0. PubMed |
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