hChT pcDNA3 Citations (2)

Originally described in: Molecular cloning of a human, hemicholinium-3-sensitive choline transporter.
Apparsundaram S, Ferguson SM, George AL, Blakely RD Biochem Biophys Res Commun. 2000 Oct 5. 276(3):862-7. PubMed Journal

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Articles Citing hChT pcDNA3

Articles
The novel p.Ser263Phe mutation in the human high-affinity choline transporter 1 (CHT1/SLC5A7) causes a lethal form of fetal akinesia syndrome. Banerjee M, Arutyunov D, Brandwein D, Janetzki-Flatt C, Kolski H, Hume S, Leonard NJ, Watt J, Lacson A, Baradi M, Leslie EM, Cordat E, Caluseriu O. Hum Mutat. 2019 Oct;40(10):1676-1683. doi: 10.1002/humu.23828. Epub 2019 Jul 12. PubMed
Biochemical characterization of two novel mutations in the human high-affinity choline transporter 1 identified in a patient with congenital myasthenic syndrome. Rizvi M, Truong TK, Zhou J, Batta M, Moran ES, Pappas J, Chu ML, Caluseriu O, Evrony GD, Leslie EM, Cordat E. Hum Mol Genet. 2023 Jan 5:ddac309. doi: 10.1093/hmg/ddac309. PubMed

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