Familial atypical parkinsonism with rare variant in VPS35 and FBXO7 genes: A case report

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dc.contributor.authorBartonikova Terezacs
dc.contributor.authorMensikova Katerinacs
dc.contributor.authorMikulicova Lenkacs
dc.contributor.authorVodicka Radekcs
dc.contributor.authorVrtel Radekcs
dc.contributor.authorGodava Marekcs
dc.contributor.authorVastik Miroslavcs
dc.contributor.authorKaiserova Michaelacs
dc.contributor.authorOtruba Pavelcs
dc.contributor.authorDolinová Ivacs
dc.contributor.authorNevrly Martincs
dc.contributor.authorKanovsky Petrcs
dc.date.accessioned2018-09-25T11:49:38Z
dc.date.available2018-09-25T11:49:38Z
dc.date.issued2016-01-01cs
dc.format.extent7cs
dc.identifier.doi10.1097/MD.0000000000005398
dc.identifier.issn1536-5964cs
dc.identifier.urihttps://dspace.tul.cz/handle/15240/27517
dc.language.isoengcs
dc.relation.ispartofseries1cs
dc.relation.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120934/cs
dc.subjectatypical parkinsonismcs
dc.subjectFBXO7cs
dc.subjecthereditary parkinsonismcs
dc.subjectVPS35cs
dc.titleFamilial atypical parkinsonism with rare variant in VPS35 and FBXO7 genes: A case reportcs
local.identifier.publikace830
local.identifier.wok000388730500048en
local.relation.issue46cs
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