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A novel syndrome caused by the E410K amino acid substitution in the neuronal B-tubulin isotype 3

dc.contributor.authorChew S
dc.contributor.authorBalasubramanian R
dc.contributor.authorChan W
dc.contributor.authorKang PB
dc.contributor.authorAndrews C
dc.contributor.authorWebb BD
dc.contributor.authorMacKinnon SE
dc.contributor.authorEngle EC
dc.contributor.authorOystreck DT
dc.contributor.authorRankin J
dc.contributor.authorCrawford TO
dc.contributor.authorGeraaghty M
dc.contributor.authorPomeroy SL
dc.contributor.authorCrowley WF
dc.contributor.authorJabs EW
dc.contributor.authorHunter DG
dc.contributor.authorGrant PE
dc.date.accessioned2014-07-07T12:32:33Z
dc.date.available2014-07-07T12:32:33Z
dc.date.issued2013
dc.identifier.citationBrain
dc.identifier.citation136
dc.identifier.citation522
dc.identifier.citation535
dc.identifier.urihttp://hdl.handle.net/10019.1/94618
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dc.descriptionJournal Articles (subsidised)
dc.descriptionGeneeskunde en Gesondheidswetenskappe
dc.descriptionOogheelkunde
dc.publisherOXFORD UNIV PRESS, GREAT CLARENDON ST, OXFORD, ENGLAND, OX2 6DP
dc.titleA novel syndrome caused by the E410K amino acid substitution in the neuronal B-tubulin isotype 3


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