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 |
Scholia | Wikidata-based representation at Scholia |
External Resources
gro-2/83444http://resolver.sub.uni-goettingen.de/purl?gro-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