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dc.contributor.authorMasuho, Ikuo
dc.contributor.authorFang, Mingyan
dc.contributor.authorGeng, Chunyu
dc.contributor.authorZhang, Jianguo
dc.contributor.authorJiang, Hui
dc.contributor.authorÖzgul, Riza Köksal
dc.contributor.authorYılmaz, Didem Yücel
dc.contributor.authorYalnızoğlu, Dilek
dc.contributor.authorYüksel, Deniz
dc.contributor.authorYarrow, Anna
dc.contributor.authorMyers, Angela
dc.contributor.authorBurn, Sabrina C.
dc.contributor.authorCrotwell, Patricia L.
dc.contributor.authorPadilla-Lopez, Sergio
dc.contributor.authorDursun, Ali
dc.contributor.authorMartemyanov, Kirill A.
dc.contributor.authorKruer, Michael C.
dc.date.accessioned2019-12-10T10:38:37Z
dc.date.available2019-12-10T10:38:37Z
dc.date.issued2016
dc.identifier.issn2376-7839
dc.identifier.urihttps://doi.org/10.1212/NXG.0000000000000078
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4866576/
dc.identifier.urihttp://hdl.handle.net/11655/14068
dc.relation.isversionof10.1212/NXG.0000000000000078
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleHomozygous Gnal Mutation Associated With Familial Childhood-Onset Generalized Dystonia
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalNeurology: Genetics
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume2
dc.identifier.issue3
dc.description.indexPubMed


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