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Article: Aberrant phase separation and nucleolar dysfunction in rare genetic diseases

DC FieldValueLanguage
dc.contributor.authorMensah, MA-
dc.contributor.authorNiskanen, H-
dc.contributor.authorMagalhaes, AP-
dc.contributor.authorBasu, S-
dc.contributor.authorKircher, M-
dc.contributor.authorSczakiel, HL-
dc.contributor.authorReiter, AMV-
dc.contributor.authorElsner, J-
dc.contributor.authorMeinecke, P-
dc.contributor.authorBiskup, S-
dc.contributor.authorChung, BHY-
dc.contributor.authorDombrowsky, G-
dc.contributor.authorEckmann=Schoiz, C-
dc.contributor.authorHitz, MP-
dc.contributor.authorHoischen, A-
dc.contributor.authorHolterhus, PM-
dc.contributor.authorHulsemann, W-
dc.contributor.authorKahrizi, K-
dc.contributor.authorKalscheuer, VM-
dc.contributor.authorKan, SYA-
dc.contributor.authorKrumbiegel, M-
dc.contributor.authorKurth, I-
dc.contributor.authorLeubner, J-
dc.contributor.authorLongardt, AC-
dc.contributor.authorMoritz, JD-
dc.contributor.authorNajmabadi, H-
dc.contributor.authorSkipalova, K-
dc.contributor.authorSnijders, BL-
dc.contributor.authorTzschach, A-
dc.contributor.authorWiedersberg, E-
dc.contributor.authorZenker, M-
dc.contributor.authorGarcia-Cabau, C-
dc.contributor.authorBuschow, R-
dc.contributor.authorSalvatella, X-
dc.contributor.authorKraushar, ML-
dc.contributor.authorMundlos, S-
dc.contributor.authorCallebe, A-
dc.contributor.authorSpielmann, M-
dc.contributor.authorHorn, D-
dc.contributor.authorHnisz, D-
dc.date.accessioned2023-03-06T01:25:53Z-
dc.date.available2023-03-06T01:25:53Z-
dc.date.issued2023-
dc.identifier.citationNature, 2023, v. 614-
dc.identifier.urihttp://hdl.handle.net/10722/325888-
dc.languageeng-
dc.relation.ispartofNature-
dc.titleAberrant phase separation and nucleolar dysfunction in rare genetic diseases-
dc.typeArticle-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.identifier.doi10.1038/s41586-022-05682-1-
dc.identifier.hkuros344163-
dc.identifier.volume614-
dc.identifier.isiWOS:000936543100008-

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