| Property |
Value |
| Working Groups |
RG Wollnik |
| Subproject |
None |
| Open Access |
Yes |
| Publication Type |
Journal Article |
| Peer Reviewed |
Yes |
| PMID |
37131188 |
| DOI |
10.1186/s13023-023-02706-5 |
| Publication Year |
2023 |
| Title |
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued |
| Journal |
Orphanet Journal of Rare Diseases |
| eISSN |
1750-1172 |
| URL |
http://dx.doi.org/10.1186/s13023-023-02706-5 |
| Issue |
1 |
| Volume |
18 |
| Journal Abbreviation |
Orphanet J Rare Dis |
| Authors |
Schröder S, Yigit G, Li Y, Altmüller J, Büttel H, Fiedler B, Kretzschmar C, Nürnberg P, Seeger J, Serpieri V, Valente EM, Wollnik B, Boltshauser E, Brockmann K |
| First Author |
Schröder S |
| Last Author |
Brockmann K |
External Resources
ojrd.bio...-5.pdfhttps://ojrd.biomedcentral.com/counter/pdf/10.1186/s13023-023-02706-5.pdf Article fulltext
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)
0000-0001-6823-9091https://orcid.org/0000-0001-6823-9091 ORCID identifier (Knut Brockmann)
1/149https://mbexc.uni-goettingen.de/archive/1/149 Research Data Archive (supplemental material)
05xy1nn52https://ror.org/05xy1nn52 ROR identifier (05xy1nn52, Multiscale Bioimaging)
021ft0n22https://ror.org/021ft0n22 ROR identifier (021ft0n22, University Medical Center Göttingen)
goeseek.gwdguser.de/studies/44https://goeseek.gwdguser.de/studies/44 Supplemental material (goeseek study)
static-c...SM.pdfhttps://static-content.springer.com/esm/art%3A10.1186%2Fs13023-023-02706-5/MediaObjects/13023_2023_2706_MOESM1_ESM.pdf Supplemental material (table)
mbexc.de...inued/https://mbexc.de/the-genetic-spectrum-of-congenital-ocular-motor-apraxia-type-cogan-an-observational-study-continued/ Website entry (mbexc.de)