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Zebrafish: an interesting model to study CDKL5 deficiency disorder

dc.contributor.authorVarela, Tatiana
dc.contributor.authorVarela, Débora
dc.contributor.authorVitorino, Marta
dc.contributor.authorConceição, Natércia
dc.contributor.authorCancela, M. Leonor
dc.contributor.authorMartins, Gil
dc.date.accessioned2020-05-04T09:35:50Z
dc.date.available2020-05-04T09:35:50Z
dc.date.issued2020
dc.description.abstractCDKL5 deficiency disorder is a rare X-linked condition that results in early onset of impairedmotor and cognitive skills such as motor rigidity, stereotypical hand movements and deficient language acquisition aswell as recurrent seizures. It is caused by mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene, which encodes a serine/threonine kinase involved in important neuronal processes such as cell signaling and neuron morphogenesis.pt_PT
dc.description.sponsorshipFCT: UID/Multi/04326/2019 (CCMAR)pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1097/MD.0000000000019291pt_PT
dc.identifier.issn0025-7974
dc.identifier.urihttp://hdl.handle.net/10400.1/13825
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherLippincott, Williams & Wilkinspt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectZebrafishpt_PT
dc.titleZebrafish: an interesting model to study CDKL5 deficiency disorderpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.endPage17pt_PT
oaire.citation.issue9pt_PT
oaire.citation.startPage16pt_PT
oaire.citation.titleMedicinept_PT
oaire.citation.volume99pt_PT
person.familyNameDomingos Varela
person.familyNameDomingos Varela
person.familyNameVitorino
person.familyNameConceição
person.familyNameCancela
person.givenNameTatiana da Conceição
person.givenNameDébora Cristina
person.givenNameMarta
person.givenNameNatércia
person.givenNameM. Leonor
person.identifier.ciencia-idF613-7482-6731
person.identifier.ciencia-id9A1C-DFE4-98C9
person.identifier.ciencia-id4615-FF5B-E951
person.identifier.ciencia-id7C11-760D-F425
person.identifier.orcid0000-0001-8563-8975
person.identifier.orcid0000-0002-5057-0912
person.identifier.orcid0000-0003-3114-6662
person.identifier.ridU-9947-2018
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
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relation.isAuthorOfPublication.latestForDiscovery62064ac0-1f34-407d-96b7-b7074325a84e

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