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Publication
PropertyValue
Working Groups RG Wollnik
SubprojectRA1.2
Open AccessOpen Access Yes
Publication TypeJournal Article
Peer ReviewedYes
PMIDPubMed ID 34172529
DOIDOI 10.1136/jmedgenet-2021-107769
Publication Year2021
TitleLoss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state
JournalJournal of Medical Genetics
ISSN0022-2593
eISSN1468-6244
URL http://dx.doi.org/10.1136/jmedgenet-2021-107769
Pagesjmedgenet-2021-107769
Journal AbbreviationJ Med Genet
AuthorsYigit G, Sheffer R, Daana M, Li Y, Kaygusuz E, Mor-Shakad H, Altmüller J, Nürnberg P, Douiev L, Kaulfuss S, Burfeind P, Wollnik B, Brockmann K
First AuthorYigit G
Last AuthorBrockmann K

 External Resources

 jmg.bmj....ds=yes  Article fulltext

 gro-2/87729  GRO.publications identifier

 9606  NCBI taxonomy (human, Homo sapiens)

 0000-0003-2589-0364  ORCID identifier (Bernd Wollnik)

 0000-0002-7515-8596  ORCID identifier (Kathrin Brockmann)

 396  Published Data Registry entry (CRC 1002)

 05xy1nn52  ROR identifier (05xy1nn52, Multiscale Bioimaging)

 021ft0n22  ROR identifier (021ft0n22, University Medical Center Göttingen)

 SCR_010917  SciCrunch identifier (RRID:SCR_010917, Agilent CytoGenomics)

 SCR_014963  SciCrunch identifier (RRID:SCR_014963, Agilent Feature Extraction Software)

 mbexc.de...state/  Website entry (mbexc.de)