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AuthorSchubert, Juliandc.contributor.author
AuthorParavidino, Robertadc.contributor.author
AuthorBecker, Felicitasdc.contributor.author
AuthorBerger, Andreadc.contributor.author
AuthorBebek, Nersesdc.contributor.author
AuthorBianchi, Amedeodc.contributor.author
AuthorBrockmann, Knutdc.contributor.author
AuthorCapovilla, Giuseppedc.contributor.author
AuthorBernardina, Bernardo Dalladc.contributor.author
AuthorFukuyama, Yukiodc.contributor.author
AuthorHoffmann, Georg F.dc.contributor.author
AuthorJurkat-Rott, Karindc.contributor.author
AuthorAnttonen, Anna-Kaisadc.contributor.author
AuthorKurlemann, Gerharddc.contributor.author
AuthorLehesjoki, Anna-Elinadc.contributor.author
AuthorLehmann-Horn, Frankdc.contributor.author
AuthorMastrangelo, Massimodc.contributor.author
AuthorMause, Ulrikedc.contributor.author
AuthorMueller, Stephandc.contributor.author
AuthorNeubauer, Bernddc.contributor.author
AuthorPuest, Burkharddc.contributor.author
AuthorRating, Dietzdc.contributor.author
AuthorRobbiano, Angeladc.contributor.author
AuthorRuf, Susannedc.contributor.author
AuthorSchroeder, Christopherdc.contributor.author
AuthorSeidel, Andreasdc.contributor.author
AuthorSpecchio, Nicoladc.contributor.author
AuthorStephani, Ulrichdc.contributor.author
AuthorStriano, Pasqualedc.contributor.author
AuthorTeichler, Jensdc.contributor.author
AuthorTurkdogan, Dilsaddc.contributor.author
AuthorVigevano, Federicodc.contributor.author
AuthorViri, Mauriziodc.contributor.author
AuthorBauer, Peterdc.contributor.author
AuthorZara, Federicodc.contributor.author
AuthorLerche, Holgerdc.contributor.author
AuthorWeber, Yvonne G.dc.contributor.author
Date of accession2018-08-28T07:55:21Zdc.date.accessioned
Available in OPARU since2018-08-28T07:55:21Zdc.date.available
Date of first publication2012dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
Keywordsynaptic vesicledc.subject
Keywordepilepsydc.subject
Keywordchoreoathetosisdc.subject
KeywordPRRT2dc.subject
Keywordglucose-transporter glut1dc.subject
Keywordchoreoathetosis syndromedc.subject
Keywordkinesigenic dyskinesiadc.subject
Keywordchromosome 16p12-q12dc.subject
Keywordconvulsionsdc.subject
Keywordlinkagedc.subject
Keywordgenedc.subject
Keywordregiondc.subject
Keywordonsetdc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitlePRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizuresdc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Klinik für Neurologieuulm.affiliationSpecific
InstitutionNeurophysiologieuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1002/humu.22126dc.identifier.doiExternal
Source - Title of sourceHuman Mutationsource.title
Source - Place of publicationWileysource.publisher
Source - Volume33source.volume
Source - Issue10source.issue
Source - Year2012source.year
Source - From page1439source.fromPage
Source - To page1443source.toPage
Source - ISSN1059-7794source.identifier.issn
FundingNational Genome Network of the Federal Ministry for Education and Research [BMBF: NGFNplus/01GS08123]uulm.funding
FundingEuropean Union [Epicure: LSH 037315]uulm.funding
Open AccessNouulm.OA
Suitable communityUniversitätsklinikum Ulmuulm.community
WoS000308714500008uulm.identifier.wos


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