Gain-Of-Function Mutations in Ifih1 Cause a Spectrum of Human Disease Phenotypes Associated with Upregulated Type I Interferon Signaling

AuthID
P-009-DE6
53
Author(s)
Jenkinson, EM
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Forte, GMA
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Anderson, BH
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[+4]·
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[+2]·
[+3]·
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[+11]·
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Wolfe, LA
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Hur, S
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Document Type
Article
Year published
2014
Published
in NATURE GENETICS, ISSN: 1061-4036
Volume: 46, Issue: 5, Pages: 503-509 (7)
Indexing
Publication Identifiers
Pubmed: 24686847
Scopus: 2-s2.0-84899495767
Wos: WOS:000335422900020
Source Identifiers
ISSN: 1061-4036
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Name Order Name   Name Order Name   Name Order Name
1 Rice, GI;   2 Duany, YD;   3 Jenkinson, EM;
4 Forte, GMA;   5 Anderson, BH;   6 Ariaudo, G;
7 Bader Meunier, B;   8 Baildam, EM;   9 Battini, R;
10 Beresford, MW;   11 Casarano, M;   12 Chouchane, M;
13 Cimaz, R;   14 Collins, AE;   15 Cordeiro, NJV;
16 Dale, RC;   17 Davidson, JE;   18 De Waele, L;
19 Desguerre, I;   20 Faivre, L;   21 Fazzi, E;
22 Isidor, B;   23 Lagae, L;   24 Latchman, AR;
25 Lebon, P;   26 Li, CM;   27 Livingston, JH;
28 Lourenco, CM;   29 Mancardi, MM;   30 Masurel Paulet, A;
31 McInnes, LB;   32 Menezes, MP;   33 Mignot, C;
34 O'Sullivan, J;   35 Orcesi, S;   36 Picco, PP;
37 Riva, E;   38 Robinson, RA;   39 Rodriguez, D;
40 Salvatici, E;   41 Scott, C;   42 Szybowska, M;
43 Tolmie, JL;   44 Vanderver, A;   45 Vanhulle, C;
46 Vieira, JP;   47 Webb, K;   48 Whitney, RN;
49 Williams, SG;   50 Wolfe, LA;   51 Zuberi, SM;
52 Hur, S;   53 Grow, YJ;