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Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2
38 auth.
C. Duncan,
B. Thompson,
Rui Chen,
G. Rice,
F. Gothe,
D. Young,
S. Lovell,
V. Shuttleworth,
V. Brocklebank,
Bronte M. Corner,
A. Skelton,
V. Bondet,
J. Coxhead,
D. Duffy,
C. Fourrage,
...
J. Livingston,
J. Pavaine,
E. Cheesman,
Stephania Bitetti,
Angela Grainger,
M. Acres,
B. Innes,
A. Mikulasova,
Ruyue Sun,
Rafiqul Hussain,
R. Wright,
R. Wynn,
M. Zarhrate,
L. Zeef,
K. Wood,
S. Hughes,
C. Harris,
Karin R. Engelhardt,
Y. Crow,
R. Randall,
D. Kavanagh,
S. Hambleton,
T. Briggs
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6 |
2019 |
6 🐜
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