| Property |
Value |
| Working Groups |
RG Wollnik |
| Subproject |
None |
| Open Access |
Yes |
| Publication Type |
Journal Article |
| Peer Reviewed |
Yes |
| PMID |
34629465 |
| DOI |
10.1038/s41431-021-00967-x |
| Publication Year |
2021 |
| Title |
Familial cleft tongue caused by a unique translation initiation codon variant in TP63 |
| Journal |
European Journal of Human Genetics |
| ISSN |
1018-4813 |
| eISSN |
1476-5438 |
| URL |
http://dx.doi.org/10.1038/s41431-021-00967-x |
| Journal Abbreviation |
Eur J Hum Genet |
| Authors |
Schmidt J, Schreiber G, Altmüller J, Thiele H, Nürnberg P, Li Y, Kaulfuß S, Funke R, Wilken B, Yigit G, Wollnik B |
| First Author |
Schmidt J |
| Last Author |
Wollnik B |
External Resources
nature.c...-x.pdfhttps://www.nature.com/articles/s41431-021-00967-x.pdf Article fulltext
2/94604https://publications.goettingen-research-online.de/handle/2/94604 GRO.publications identifier
9606https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id=9606 NCBI taxonomy (human, Homo sapiens)
0000-0002-5942-2924https://orcid.org/0000-0002-5942-2924 ORCID identifier (Julia Schmidt)
0000-0003-2777-0198https://orcid.org/0000-0003-2777-0198 ORCID identifier (Gökhan Yigit)
0000-0003-2589-0364https://orcid.org/0000-0003-2589-0364 ORCID identifier (Bernd Wollnik)
0493xsw21https://ror.org/0493xsw21 ROR identifier (0493xsw21, Berlin Institute of Health at Charité - Universitätsmedizin Berlin)
048ycfv73https://ror.org/048ycfv73 ROR identifier (048ycfv73, Klinikum Kassel)
04p5ggc03https://ror.org/04p5ggc03 ROR identifier (04p5ggc03, Max Delbrück Center for Molecular Medicine)
05xy1nn52https://ror.org/05xy1nn52 ROR identifier (05xy1nn52, Multiscale Bioimaging)
05mxhda18https://ror.org/05mxhda18 ROR identifier (05mxhda18, University Hospital Cologne)
021ft0n22https://ror.org/021ft0n22 ROR identifier (021ft0n22, University Medical Center Göttingen)
SCR_018393https://scicrunch.org/resolver/SCR_018393 SciCrunch identifier (RRID:SCR_018393, Combined Annotation Dependent Depletion)
SCR_002344https://scicrunch.org/resolver/SCR_002344 SciCrunch identifier (RRID:SCR_002344, Ensembl)
SCR_014964https://scicrunch.org/resolver/SCR_014964 SciCrunch identifier (RRID:SCR_014964, Genome Aggregation Database)
SCR_001888https://scicrunch.org/resolver/SCR_001888 SciCrunch identifier (RRID:SCR_001888, HGMD)
SCR_016386https://scicrunch.org/resolver/SCR_016386 SciCrunch identifier (RRID:SCR_016386, Illumina HiSeq 3000/HiSeq 4000 System)
SCR_010777https://scicrunch.org/resolver/SCR_010777 SciCrunch identifier (RRID:SCR_010777, MutationTaster)
SCR_006472https://scicrunch.org/resolver/SCR_006472 SciCrunch identifier (RRID:SCR_006472, NCBI)
SCR_013189https://scicrunch.org/resolver/SCR_013189 SciCrunch identifier (RRID:SCR_013189, PolyPhen)
SCR_012813https://scicrunch.org/resolver/SCR_012813 SciCrunch identifier (RRID:SCR_012813, SIFT)
SCR_005780https://scicrunch.org/resolver/SCR_005780 SciCrunch identifier (RRID:SCR_005780, UCSC Genome Browser)
mbexc.de...-tp63/https://mbexc.de/familial-cleft-tongue-caused-by-a-unique-translation-initiation-codon-variant-in-tp63/ Website entry (mbexc.de)
Q112812680https://www.wikidata.org/wiki/Q112812680 Wikidata ID