| Property |
Value |
| Working Groups |
RG Wollnik |
| Subproject |
RA1.1 |
| Open Access |
No |
| Publication Type |
Journal Article |
| Peer Reviewed |
Yes |
| PMID |
33283961 |
| DOI |
10.1002/ajmg.a.62009 |
| Publication Year |
2020 |
| Title |
Aplasia cutis congenita in a CDC42‐related developmental phenotype |
| Journal |
American Journal of Medical Genetics Part A |
| ISSN |
1552-4825 |
| eISSN |
1552-4833 |
| URL |
http://dx.doi.org/10.1002/ajmg.a.62009 |
| Journal Abbreviation |
Am J Med Genet A |
| Authors |
Schnabel F, Kamphausen SB, Funke R, Kaulfuß S, Wollnik B, Zenker M |
| First Author |
Schnabel F |
| Last Author |
Zenker M |
External Resources
2/83444https://publications.goettingen-research-online.de/handle/2/83444 GRO.publications identifier
NP_001782.1https://www.ncbi.nlm.nih.gov/protein/NP_001782.1 NCBI protein (NP_001782.1)
9606https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id=9606 NCBI taxonomy (human, Homo sapiens)
0000-0003-2589-0364https://orcid.org/0000-0003-2589-0364 ORCID identifier (Bernd Wollnik)
05xy1nn52https://ror.org/05xy1nn52 ROR identifier (05xy1nn52, Multiscale Bioimaging)
03m04df46https://ror.org/03m04df46 ROR identifier (03m04df46, University Hospital Magdeburg)
021ft0n22https://ror.org/021ft0n22 ROR identifier (021ft0n22, University Medical Center Göttingen)
SCR_016379https://scicrunch.org/resolver/SCR_016379 SciCrunch identifier (RRID:SCR_016379, Illumina MiSeq System)
SCR_016381https://scicrunch.org/resolver/SCR_016381 SciCrunch identifier (RRID:SCR_016381, Illumina NextSeq sequencer)
mbexc.de...otype/https://mbexc.de/aplasia-cutis-congenita-in-a-cdc42-related-developmental-phenotype/ Website entry (mbexc.de)
Q104103955https://www.wikidata.org/wiki/Q104103955 Wikidata ID