Papers: 10.1186/s40478-021-01121-w

https://doi.org/10.1186/s40478-021-01121-w

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease

Cited by: 20
Author(s): Stefanie Smolders, Stéphanie Philtjens, David Crosiers, Anne Sieben, Elisabeth Hens, Bavo Heeman, Sara Van Mossevelde, Philippe Pals, Bob Asselbergh, Roberto A. Dias, Yannick Vermeiren, Rik Vandenberghe, Sebastiaan Engelborghs, Peter Paul De Deyn, Jean‐Jacques Martin, Patrick Cras, Wim Annaert, Christine Van Broeckhoven
Published: over 5 years ago

Software Mentions 1

cran: SKAT
SNP-Set (Sequence) Kernel Association Test
Papers that mentioned: 407
Very Likely Science (83)