Ankur Chaurasia

Search results

• 2024

  Bi-allelic loss-of-function variants of FILIP1 encoding a filamin A binding protein cause autosomal recessive arthrogryposis multiplex congenita with microcephaly

  Schnabel, F., Schuler, E., Al-Maawali, A., Chaurasia, A., Syrbe, S., Al-Kindi, A., Bhavani, G., Shukla, A., Altmüller, J., Nürnberg, P., Banka, S., Girisha, K., Li, Y., Wollnik, B. & Yigit, G., Jan 2024, In: European Journal of Human Genetics. 32, p. 520-520 1 p.

  Research output: Contribution to journal › Meeting Abstract › peer-review