Vaiman, E.E.,
Shnayder, N.A.,
Zhuravlev, N.M.,
Petrova, M.M.,
Asadullin, A.R.,
Al-Zamil, M.,
Garganeeva, N.R.,
Shipulin, G.A.,
Cumming, G.,
Nasyrova, R.F. (2022) predisposition to AP-induced LQTS may be due to several causes, including
causal mutations in the
genesIdiiatullina, Elina,
Al-Azab, Mahmoud,
Lin, Meng,
Hrovat-Schaale, Katja,
Liu, Ziyang,
Li, Xiaotian,
Guo, Caiqin,
Chen, Xixi,
Li, Yaoying,
Gao, Song,
Cui, Jun,
Zhou, Wenhao,
Liu, Li,
Zhang, Yuxia,
Masters, Seth L. (2024) , and autoinflammatory disease due to type I IFN. Here, we show that a dominant negative mutation in the
gene encoding