| 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)
