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Article: GRIN2A-related disorders: genotype and functional consequence predict phenotype

DC FieldValueLanguage
dc.contributor.authorStrehlow, V-
dc.contributor.authorHeyne, HO-
dc.contributor.authorVlaskamp, DRM-
dc.contributor.authorMarwick, KFM-
dc.contributor.authorRudolf, G-
dc.contributor.authorde Bellescize, J-
dc.contributor.authorBiskup, S-
dc.contributor.authorBrilstra, EH-
dc.contributor.authorBrouwer, OF-
dc.contributor.authorCallenbach, PMC-
dc.contributor.authorHentschel, J-
dc.contributor.authorHirsch, E-
dc.contributor.authorKind, PC-
dc.contributor.authorMignot, C-
dc.contributor.authorPlatzer, K-
dc.contributor.authorRump, P-
dc.contributor.authorSkehel, PA-
dc.contributor.authorWyllie, DJA-
dc.contributor.authorHardingham, GE-
dc.contributor.authorvan Ravenswaaj-Aris, CMA-
dc.contributor.authorLesca, G-
dc.contributor.authorLemke, JR-
dc.contributor.authorArzimanoglou, A-
dc.contributor.authorAugustijn, PB-
dc.contributor.authorVan Bogaert, P-
dc.contributor.authorBourry, H-
dc.contributor.authorBurfeind, P-
dc.contributor.authorChu, WY-
dc.contributor.authorChung, BHY-
dc.contributor.authorDoummar, D-
dc.contributor.authorEdery, P-
dc.contributor.authorFattai-Valevski, A-
dc.contributor.authorFradin, M-
dc.contributor.authorGerard, M-
dc.contributor.authorde Geus, C-
dc.contributor.authorGunning, S-
dc.contributor.authorHasaerts, D-
dc.contributor.authorHelbig, I-
dc.contributor.authorHeibig, KL-
dc.contributor.authorJamra, R-
dc.contributor.authorLyver, MJ-
dc.contributor.authorWassink-Ruifer, JSK-
dc.contributor.authorKoolen, DA-
dc.contributor.authorLederer, D-
dc.contributor.authorLunsing, RJ-
dc.contributor.authorMathot, M-
dc.contributor.authorMaurey, H-
dc.contributor.authorManascu, S-
dc.contributor.authorMishel, A-
dc.contributor.authorMirzaa, G-
dc.contributor.authorMittler, D-
dc.contributor.authorMuhie, H-
dc.contributor.authorMalter, RS-
dc.contributor.authorNava, C-
dc.contributor.authorO'Brien, M-
dc.contributor.authorvan Piruderen-Nagler, E-
dc.contributor.authorvan Riesen, A-
dc.contributor.authorRougeot, C-
dc.contributor.authorSariaville, D-
dc.contributor.authorSchieving, JH-
dc.contributor.authorSyrte, S-
dc.contributor.authorVeenstra-Knol, HE-
dc.contributor.authorVerbeek, N-
dc.contributor.authorVille, D-
dc.contributor.authorVos, YJ-
dc.contributor.authorVrielynck, P-
dc.contributor.authorWagner, S-
dc.contributor.authorWeckhuysen, S-
dc.contributor.authorWillemsen, MH-
dc.date.accessioned2019-03-18T04:20:23Z-
dc.date.available2019-03-18T04:20:23Z-
dc.date.issued2019-
dc.identifier.citationBrain, 2019, v. 142, p. 80-92-
dc.identifier.issn0006-8950-
dc.identifier.urihttp://hdl.handle.net/10722/268188-
dc.languageeng-
dc.publisherOxford University Press. The Journal's web site is located at http://brain.oxfordjournals.org/-
dc.relation.ispartofBrain-
dc.rightsPost-print: This is a pre-copy-editing, author-produced PDF of an article accepted for publication in [Brain] following peer review. The definitive publisher-authenticated version [Brain, 2019, v. 142, p. 80-92] is available online at: http://brain.oxfordjournals.org/ [http://dx.doi.org/10.1093/brain/awy304].-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectchannelopathy-
dc.subjectchildhood epilepsy-
dc.subjectlearning disability-
dc.subjectmolecular genetics-
dc.subjectspike-wave EEG-
dc.titleGRIN2A-related disorders: genotype and functional consequence predict phenotype-
dc.typeArticle-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1093/brain/awy304-
dc.identifier.scopuseid_2-s2.0-85059272679-
dc.identifier.hkuros297044-
dc.identifier.volume142-
dc.identifier.spage80-
dc.identifier.epage92-
dc.identifier.isiWOS:000462617100015-
dc.publisher.placeUnited Kingdom-
dc.identifier.f1000734628231-
dc.identifier.issnl0006-8950-

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