| 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
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)
