A Rare Heterozygous Trem2 Coding Variant Identified in Familial Clustering of Dementia Affects an Intrinsically Disordered Protein Region and Function of Trem2

AuthID
P-015-P9N
29
Author(s)
Karsak M.
·
Glebov K.
·
Scheffold M.
·
Bajaj T.
·
Kawalia A.
·
Karaca I.
·
Rading S.
·
Kornhuber J.
·
Peters O.
·
Diez-Fairen M.
·
[+2]·
[+7]·
Lennarz M.
·
Jessen F.
·
Maier W.
·
Kubisch C.
·
Ignatova Z.
·
Nürnberg P.
·
Pastor P.
·
Walter J.
·
Ramirez A.
Document Type
Article
Year published
2020
Published
in Human Mutation, ISSN: 10597794
Volume: 41, Issue: 1, Pages: 169-181 (12)
Indexing
Publication Identifiers
Pubmed: 31464095
SCOPUS: 2-s2.0-85073772036
Source Identifiers
ISSN: 10597794
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Name Order Name   Name Order Name   Name Order Name
1 Karsak M.;   2 Glebov K.;   3 Scheffold M.;
4 Bajaj T.;   5 Kawalia A.;   6 Karaca I.;
7 Rading S.;   8 Kornhuber J.;   9 Peters O.;
10 Diez-Fairen M.;   11 Frölich L.;   12 Hüll M.;
13 Wiltfang J.;   14 Scherer M.;   15 Riedel-Heller S.;
16 Schneider A.;   17 Heneka M.T.;   18 Fliessbach K.;
19 Sharaf A.;   20 Thiele H.;   21 Lennarz M.;
22 Jessen F.;   23 Maier W.;   24 Kubisch C.;
25 Ignatova Z.;   26 Nürnberg P.;   27 Pastor P.;
28 Walter J.;   29 Ramirez A.;