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For: Kessi M, Chen B, Peng J, Tang Y, Olatoutou E, He F, Yang L, Yin F. Intellectual Disability and Potassium Channelopathies: A Systematic Review. Front Genet 2020;11:614. [PMID: 32655623 DOI: 10.3389/fgene.2020.00614] [Cited by in Crossref: 7] [Cited by in F6Publishing: 12] [Article Influence: 3.5] [Reference Citation Analysis]
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8 Jackson A, Banka S, Stewart H, Robinson H, Lovell S, Clayton-Smith J; Genomics England Research Consortium. Recurrent KCNT2 missense variants affecting p.Arg190 result in a recognizable phenotype. Am J Med Genet A 2021. [PMID: 34061450 DOI: 10.1002/ajmg.a.62370] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Kessi M, Chen B, Peng J, Yan F, Yang L, Yin F. Calcium channelopathies and intellectual disability: a systematic review. Orphanet J Rare Dis 2021;16:219. [PMID: 33985586 DOI: 10.1186/s13023-021-01850-0] [Cited by in F6Publishing: 5] [Reference Citation Analysis]
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11 Jerng HH, Patel JM, Khan TA, Arenkiel BR, Pfaffinger PJ. Light-regulated voltage-gated potassium channels for acute interrogation of channel function in neurons and behavior. PLoS One 2021;16:e0248688. [PMID: 33755670 DOI: 10.1371/journal.pone.0248688] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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