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CDKL5 variants: Improving our understanding of a rare neurologic disorder.
Hector RD, Kalscheuer VM, Hennig F, Leonard H, Downs J, Clarke A, Benke TA, Armstrong J, Pineda M, Bailey MES, Cobb SR. Hector RD, et al. Among authors: cobb sr. Neurol Genet. 2017 Dec 15;3(6):e200. doi: 10.1212/NXG.0000000000000200. eCollection 2017 Dec. Neurol Genet. 2017. PMID: 29264392 Free PMC article.
Characterisation of CDKL5 Transcript Isoforms in Human and Mouse.
Hector RD, Dando O, Landsberger N, Kilstrup-Nielsen C, Kind PC, Bailey ME, Cobb SR. Hector RD, et al. Among authors: cobb sr. PLoS One. 2016 Jun 17;11(6):e0157758. doi: 10.1371/journal.pone.0157758. eCollection 2016. PLoS One. 2016. PMID: 27315173 Free PMC article.
Characterisation of Cdkl5 transcript isoforms in rat.
Hector RD, Dando O, Ritakari TE, Kind PC, Bailey ME, Cobb SR. Hector RD, et al. Among authors: cobb sr. Gene. 2017 Mar 1;603:21-26. doi: 10.1016/j.gene.2016.12.001. Epub 2016 Dec 7. Gene. 2017. PMID: 27940108 Free article.
Rett syndrome: from bed to bench.
Weng SM, Bailey ME, Cobb SR. Weng SM, et al. Among authors: cobb sr. Pediatr Neonatol. 2011 Dec;52(6):309-16. doi: 10.1016/j.pedneo.2011.08.002. Epub 2011 Nov 6. Pediatr Neonatol. 2011. PMID: 22192257 Free article. Review.
98 results