General References
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- Partiseti M, Collura V, Agnel M, Culouscou JM, Graham D: Cloning and characterization of a novel human inwardly rectifying potassium channel predominantly expressed in small intestine. FEBS Lett. 1998 Aug 28;434(1-2):171-6. [PubMed:9738472 ]
- Krapivinsky G, Medina I, Eng L, Krapivinsky L, Yang Y, Clapham DE: A novel inward rectifier K+ channel with unique pore properties. Neuron. 1998 May;20(5):995-1005. [PubMed:9620703 ]
- Derst C, Doring F, Preisig-Muller R, Daut J, Karschin A, Jeck N, Weber S, Engel H, Grzeschik KH: Partial gene structure and assignment to chromosome 2q37 of the human inwardly rectifying K+ channel (Kir7.1) gene (KCNJ13). Genomics. 1998 Dec 15;54(3):560-3. [PubMed:9878260 ]
- Hejtmancik JF, Jiao X, Li A, Sergeev YV, Ding X, Sharma AK, Chan CC, Medina I, Edwards AO: Mutations in KCNJ13 cause autosomal-dominant snowflake vitreoretinal degeneration. Am J Hum Genet. 2008 Jan;82(1):174-80. doi: 10.1016/j.ajhg.2007.08.002. [PubMed:18179896 ]
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