, the search for
mutations in these genes is promising. Conclusion Most patients with NF1 develop orthopedic
of information. Results and discussion
Mutations in proinflammatory cytokine and receptor genes, metalloprotease
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 genes