Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita
2022 | preprint
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Cite this publication
Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita
Schnabel, F.; Schuler, E.; Al-Maawali, A.; Chaurasia, A.; Syrbe, S.; Al-Kindi, A.& Bhav, G. S. et al. (2022). DOI: https://doi.org/10.21203/rs.3.rs-2121654/v1
Documents & Media
Details
- Authors
- Schnabel, Franziska; Schuler, Elisabeth; Al-Maawali, Almundher; Chaurasia, Ankur; Syrbe, Steffen; Al-Kindi, Adila; Bhav, Gandham SriLakshmi; Shukla, Anju; Altmüller, Janine; Nürnberg, Peter; Banka, Siddharth; Girisha, Katta M; Li, Yun; Wollnik, Bernd ; Yigit, Gökhan
- Issue Date
- 2022
- Project
- EXC 2067: Multiscale Bioimaging
- Working Group
- RG Wollnik
