Loss-Of-Function Mutations in Hint1 Cause Axonal Neuropathy with Neuromyotonia

AuthID
P-002-4TT
37
Author(s)
Baets, J
·
Almeida Souza, L
·
De Vriendt, E
·
Matur, Z
·
Tournev, I
·
[+17]·
Peeters, K
·
Ooms, T
·
Hahn, AF
·
Zuechner, S
·
Timmerman, V
·
Van Dijck, P
·
Rasic, VM
·
Janecke, AR
·
De Jonghe, P
·
Jordanova, A
Document Type
Article
Year published
2012
Published
in NATURE GENETICS, ISSN: 1061-4036
Volume: 44, Issue: 10, Pages: 1080-1083 (4)
Indexing
Publication Identifiers
Pubmed: 22961002
Scopus: 2-s2.0-84866840027
Wos: WOS:000309550200005
Source Identifiers
ISSN: 1061-4036
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Name Order Name   Name Order Name   Name Order Name
1 Zimon, M;   2 Baets, J;   3 Almeida Souza, L;
4 De Vriendt, E;   5 Nikodinovic, J;   6 Parman, Y;
7 Battaloglu, E;   8 Matur, Z;   9 Guergueltcheva, V;
10 Tournev, I;   11 Auer Grumbach, M;   12 De Rijk, P;
13 Petersen, BS;   14 Mueller, T;   15 Fransen, E;
16 Van Damme, P;   17 Loescher, WN;   18 Barisic, N;
19 Mitrovic, Z;   20 Previtali, SC;   21 Topaloglu, H;
22 Bernert, G;   23 Beleza Meireles, A;   24 Todorovic, S;
25 Savic Pavicevic, D;   26 Ishpekova, B;   27 Lechner, S;
28 Peeters, K;   29 Ooms, T;   30 Hahn, AF;
31 Zuechner, S;   32 Timmerman, V;   33 Van Dijck, P;
34 Rasic, VM;   35 Janecke, AR;   36 De Jonghe, P;
37 Jordanova, A;