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Cited by in F6Publishing
For: 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 Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Álvarez-mora MI, Sánchez A, Rodríguez-revenga L, Corominas J, Rabionet R, Puig S, Madrigal I. Diagnostic yield of next-generation sequencing in 87 families with neurodevelopmental disorders. Orphanet J Rare Dis 2022;17. [DOI: 10.1186/s13023-022-02213-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]