h1

h2

h3

h4

h5
h6
001023232 001__ 1023232
001023232 005__ 20251222095353.0
001023232 0247_ $$2ISSN$$a1018-4813
001023232 0247_ $$2ISSN$$a1476-5438
001023232 0247_ $$2WOS$$aWOS:001421430500825
001023232 037__ $$aRWTH-2025-10588
001023232 041__ $$aEnglish
001023232 082__ $$a610
001023232 1001_ $$aLassuthova, Petra$$b0
001023232 1112_ $$a57. Conference of the European-Society-of-Human-Genetics$$cBerlin$$d2024-06-01 - 2024-06-04$$gESHG 2024$$wGermany
001023232 245__ $$aBiallelic variants in the neuronal isoform of the DST gene as a cause of hereditary sensory neuropathy$$honline, print
001023232 260__ $$aBasingstoke$$bStockton Press$$c2024
001023232 300__ $$a1099-1099
001023232 3367_ $$00$$2EndNote$$aJournal Article
001023232 3367_ $$0PUB:(DE-HGF)1$$2PUB:(DE-HGF)$$aAbstract
001023232 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal
001023232 3367_ $$0PUB:(DE-HGF)8$$2PUB:(DE-HGF)$$aContribution to a conference proceedings
001023232 3367_ $$2BibTeX$$aARTICLE
001023232 3367_ $$2DRIVER$$aarticle
001023232 3367_ $$2DataCite$$aOutput Types/Journal article
001023232 3367_ $$2ORCID$$aJOURNAL_ARTICLE
001023232 500__ $$ae-Poster abstract. - In Artikel: Abstracts from the 57th European Society of Human Genetics (ESHG) Conference: e-Posters. - Seiten 904–1230
001023232 591__ $$aCzech Republic
001023232 591__ $$aGermany
001023232 7001_ $$aGrecmalova, Dagmar$$b1
001023232 7001_ $$0P:(DE-82)987556$$aLischka, Annette$$b2$$urwth
001023232 7001_ $$0P:(DE-82)027621$$aEggermann, Katja$$b3$$urwth
001023232 7001_ $$0P:(DE-82)IDM06155$$aKurth, Ingo$$b4$$urwth
001023232 7001_ $$aMazanec, Radim$$b5
001023232 770__ $$aAbstracts from the 57th European Society of Human Genetics (ESHG) Conference
001023232 773__ $$0PERI:(DE-600)2005160-8$$nSupplement 2$$pEP12.020$$tEuropean journal of human genetics$$v32$$x1018-4813$$y2024
001023232 8564_ $$uhttps://doi.org/10.1038/s41431-024-01733-5$$yHomepage of journal
001023232 909CO $$ooai:publications.rwth-aachen.de:1023232$$pVDB
001023232 9151_ $$0StatID:(DE-HGF)0021$$2StatID$$aNo peer reviewed article$$x0
001023232 915__ $$0StatID:(DE-HGF)0030$$2StatID$$aPeer Review$$bASC$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)0100$$2StatID$$aJCR$$bEUR J HUM GENET : 2022$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)0113$$2StatID$$aWoS$$bScience Citation Index Expanded$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)0150$$2StatID$$aDBCoverage$$bWeb of Science Core Collection$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)0160$$2StatID$$aDBCoverage$$bEssential Science Indicators$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)0199$$2StatID$$aDBCoverage$$bClarivate Analytics Master Journal List$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)0200$$2StatID$$aDBCoverage$$bSCOPUS$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)0300$$2StatID$$aDBCoverage$$bMedline$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)0600$$2StatID$$aDBCoverage$$bEbsco Academic Search$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)1030$$2StatID$$aDBCoverage$$bCurrent Contents - Life Sciences$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)1050$$2StatID$$aDBCoverage$$bBIOSIS Previews$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)1190$$2StatID$$aDBCoverage$$bBiological Abstracts$$d2024-12-27
001023232 915__ $$0StatID:(DE-HGF)3002$$2StatID$$aDEAL Springer$$d2024-12-27$$wger
001023232 915__ $$0StatID:(DE-HGF)9905$$2StatID$$aIF >= 5$$bEUR J HUM GENET : 2022$$d2024-12-27
001023232 9141_ $$y2024
001023232 9101_ $$0I:(DE-588b)36225-6$$6P:(DE-82)987556$$aRWTH Aachen$$b2$$kRWTH
001023232 9101_ $$0I:(DE-588b)36225-6$$6P:(DE-82)027621$$aRWTH Aachen$$b3$$kRWTH
001023232 9101_ $$0I:(DE-588b)36225-6$$6P:(DE-82)IDM06155$$aRWTH Aachen$$b4$$kRWTH
001023232 9201_ $$0I:(DE-82)525000-2_20140620$$k924610$$lInstitut und Lehrstuhl für Humangenetik und Genommedizin$$x0
001023232 961__ $$c2025-12-10T14:50:10.648427$$x2025-12-10T14:50:10.648427$$z2025-12-10T14:50:10.648427
001023232 980__ $$aI:(DE-82)525000-2_20140620
001023232 980__ $$aUNRESTRICTED
001023232 980__ $$aVDB
001023232 980__ $$aabstract
001023232 980__ $$acontrib
001023232 980__ $$ajournal