Transcript-specific loss-of-function variants in VPS16 are enriched in patients with dystonia - Park, Joohyun; Reilaender, Annemarie; Petry-Schmelzer, Jan N.; Stöbe, Petra; Cordts, Isabell; Harmuth, Florian; Rautenberg, Maren; Woerz, Sarah E.; Demidov, German; Sturm, Marc; Ossowski, Stephan; Schwaibold, Eva; et al. (Neurology. Genetics, 2022)
First published December 7, 2021