ORCID
- Glebov, Konstantin: 0000-0001-9023-7076
DOI
10.1002/humu.23904
Publication Date
2019-08-25
Publication Title
Human Mutation
ISSN
1059-7794
Embargo Period
2019-12-18
Organisational Unit
Peninsula Medical School
Recommended Citation
Karsak, M., Glebov, K., Scheffold, M., Bajaj, T., Kawalia, A., Karaca, I., Rading, S., Kornhuber, J., Peters, O., Diez‐Fairen, M., Frölich, L., Hüll, M., Wiltfang, J., Scherer, M., Riedel‐Heller, S., Schneider, A., Heneka, M., Fliessbach, K., Sharaf, A., Thiele, H., Lennarz, M., Jessen, F., Maier, W., Kubisch, C., Ignatova, Z., Nürnberg, P., Pastor, P., Walter, J., & Ramirez, A. (2019) 'A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2', Human Mutation, . Available at: https://doi.org/10.1002/humu.23904
