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Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's Syndrome

dc.contributor.authorPlaster, N
dc.contributor.authorDeymeer, F
dc.contributor.authorGeorge, A
dc.contributor.authorHahn, A
dc.contributor.authorNitu, A
dc.contributor.authorSerdaroglu, P
dc.contributor.authorSubramony, SH
dc.contributor.authorWolfe, G
dc.contributor.authorFu, YH
dc.contributor.authorPtacek, LJ
dc.contributor.authorTawil, R
dc.contributor.authorTristani-Firouzi, M
dc.contributor.authorCanun, S
dc.contributor.authorBendahhou, S
dc.contributor.authorSoemori, A
dc.contributor.authorDonaldson, MR
dc.contributor.authorIannaccone, S
dc.contributor.authorBrunt, E
dc.contributor.authorBarohn, R
dc.contributor.authorClark, J
dc.date.accessioned2021-03-04T14:47:43Z
dc.date.available2021-03-04T14:47:43Z
dc.identifier.citationPlaster N., Tawil R., Tristani-Firouzi M., Canun S., Bendahhou S., Soemori A., Donaldson M., Iannaccone S., Brunt E., Barohn R., et al., "Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's Syndrome", NEUROMUSCULAR DISORDERS, cilt.11, ss.667-668, 2001
dc.identifier.issn0960-8966
dc.identifier.othervv_1032021
dc.identifier.otherav_83647ccc-1d73-4d17-b412-29dbdd71e1e8
dc.identifier.urihttp://hdl.handle.net/20.500.12627/89433
dc.language.isoeng
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectSinirbilim ve Davranış
dc.subjectNEUROSCIENCES
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleMutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's Syndrome
dc.typeMakale
dc.relation.journalNEUROMUSCULAR DISORDERS
dc.contributor.department, ,
dc.identifier.volume11
dc.identifier.startpage667
dc.identifier.endpage668
dc.contributor.firstauthorID163034


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