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Genetic and clinical variations in a Norwegian sample diagnosed with Rett syndrome.
Henriksen MW, Breck H, Sejersted Y, Diseth T, von Tetzchner S, Paus B, Skjeldal OH. Henriksen MW, et al. Brain Dev. 2020 Aug;42(7):484-495. doi: 10.1016/j.braindev.2020.03.008. Epub 2020 Apr 23. Brain Dev. 2020. PMID: 32336485
Epilepsy in classic Rett syndrome: Course and characteristics in adult age.
Henriksen MW, Breck H, von Tetzchner S, Paus B, Skjeldal OH, Brodtkorb E. Henriksen MW, et al. Epilepsy Res. 2018 Sep;145:134-139. doi: 10.1016/j.eplepsyres.2018.06.012. Epub 2018 Jun 23. Epilepsy Res. 2018. PMID: 29966812
De novo mutations in SCN1A are associated with classic Rett syndrome: a case report.
Henriksen MW, Ravn K, Paus B, von Tetzchner S, Skjeldal OH. Henriksen MW, et al. BMC Med Genet. 2018 Oct 11;19(1):184. doi: 10.1186/s12881-018-0700-z. BMC Med Genet. 2018. PMID: 30305042 Free PMC article.
Medical Issues in Adults with Rett Syndrome - A National Survey.
Henriksen MW, Breck H, von Tetzchner S, Paus B, Skjeldal OH. Henriksen MW, et al. Dev Neurorehabil. 2020 Feb;23(2):106-112. doi: 10.1080/17518423.2019.1646341. Epub 2019 Jul 25. Dev Neurorehabil. 2020. PMID: 31342829
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