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Publication
Property Value
Working Groups RG Wollnik
Subproject None
Open Access Open Access  Yes
Publication Type Journal Article
Peer Reviewed Yes
PMID PubMed ID  37671045
DOI DOI  10.3389/fgene.2023.1214736
Publication Year 2023
Title Unraveling haplotype errors in the DFNA33 locus
Journal Frontiers in Genetics
ISSN 1664-8021
URL  http://dx.doi.org/10.3389/fgene.2023.1214736
Volume 14
Journal Abbreviation Front Genet
Authors Vona B, Regele S, Rad A, Strenzke N, Pater JA, Neumann K, Sturm M, Haack TB, Am Zehnhoff-Dinnesen AG
First Author Vona B
Last Author Am Zehnhoff-Dinnesen AG

 External Resources

 frontier...=False Article fulltext

 2/133106 GRO.publications identifier

 ENST00000375630 Ensembl identifier (ENST00000375630)

 0000-0002-6719-3447 ORCID identifier (Barbara Vona)

 0000-0003-1673-1046 ORCID identifier (Nicola Strenzke)

 0000-0002-3975-0736 ORCID identifier (Katrin Neumann)

 0000-0002-6552-8362 ORCID identifier (Marc Sturm)

 0000-0001-6033-4836 ORCID identifier (Tobias B. Haack)

 0000-0002-6146-1500 ORCID identifier (Antoinette am Zehnhoff-Dinnesen)

 1/282 Research Data Archive (supplemental material)

 03vek6s52 ROR identifier (03vek6s52, Harvard University)

 04haebc03 ROR identifier (04haebc03, Memorial University of Newfoundland)

 05xy1nn52 ROR identifier (05xy1nn52, Multiscale Bioimaging)

 01856cw59 ROR identifier (01856cw59, University Hospital Münster)

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

 03a1kwz48 ROR identifier (03a1kwz48, University of Tübingen)

 CVCL_0063 SciCrunch identifier (RRID:CVCL_0063, HEK293T)

 SCR_006169 SciCrunch identifier (RRID:SCR_006169, ClinVar)

 SCR_001888 SciCrunch identifier (RRID:SCR_001888, HGMD)

 SCR_016387 SciCrunch identifier (RRID:SCR_016387, Illumina NovaSeq 6000 Sequencing System)

 database...435034 Supplemental material

 github.com/imgag/megSAP Supplemental material (code, reused)

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

 Q125336718 Wikidata ID