Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly
- F. Schnabel
- E. Schuler
- A. Al-Maawali
- A. Chaurasia
- S. Syrbe
- A. Al-Kindi
- G.S. Bhavani
- A. Shukla
- J. Altmüller
- P. Nürnberg
- S. Banka
- K.M. Girisha
- Y. Li
- B. Wollnik
- G. Yigit