A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2

Authors

M Karsak
K Glebov, Peninsula Medical School
M Scheffold
T Bajaj
A Kawalia
I Karaca
S Rading
J Kornhuber
O Peters
M Diez‐Fairen
L Frölich
M Hüll
J Wiltfang
M Scherer
S Riedel‐Heller
A Schneider
MT Heneka
K Fliessbach
A Sharaf
H Thiele
M Lennarz
F Jessen
W Maier
C Kubisch
Z Ignatova
P Nürnberg
P Pastor
J Walter
A Ramirez

ORCID

• K Glebov: 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

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: 10.1002/humu.23904