| Property |
Value |
| Working Groups |
RG Wollnik |
| Subproject |
None |
| Open Access |
Yes |
| Publication Type |
Preprint |
| Peer Reviewed |
No |
| DOI |
10.21203/rs.3.rs-2121654/v1 |
| Publication Year |
2022 |
| Title |
Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita |
| Journal |
Researchsquare |
| URL |
http://dx.doi.org/10.21203/rs.3.rs-2121654/v1 |
| Journal Abbreviation |
Researchsquare |
| Extra |
Not yet finally published in a peer-reviewd journal. |
| Authors |
Schnabel F, Schuler E, Al-Maawali A, Chaurasia A, Syrbe S, Al-Kindi A, Bhav GS, Shukla A, Altmüller J, Nürnberg P, Banka S, Girisha KM, Li Y, Wollnik B, Yigit G |
| First Author |
Schnabel F |
| Last Author |
Yigit G |
External Resources
2/121706https://publications.goettingen-research-online.de/handle/2/121706 GRO.publications identifier
0000-0002-9966-8937https://orcid.org/0000-0002-9966-8937 ORCID identifier (Franziska Schnabel)
0000-0003-2589-0364https://orcid.org/0000-0003-2589-0364 ORCID identifier (Bernd Wollnik)
0000-0003-2777-0198https://orcid.org/0000-0003-2777-0198 ORCID identifier (Gökhan Yigit)
05xy1nn52https://ror.org/05xy1nn52 ROR identifier (05xy1nn52, Multiscale Bioimaging)
021ft0n22https://ror.org/021ft0n22 ROR identifier (021ft0n22, University Medical Center Göttingen)
mbexc.de...enita/https://mbexc.de/homozygous-loss-of-function-variants-in-filip1-cause-autosomal-recessive-arthrogryposis-multiplex-congenita/ Website entry (mbexc.de)