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) responsible for monoheme forms of LQTS, single nucleotide
variants
(SNVs) of the candidate
genes encoding
polymorphisms (SNPs), most located in intergenic and regulatory regions where many transposable element
genes Coignard, J.,
Lush, M.,
Beesley, J.,
O’Mara, T.A.,
Dennis, J,
Tyrer, J.P.,
Barnes, D.R.,
McGuffog, L.,
Leslie, G.,
Bolla, M.K.,
Adank, M.A.,
Kiiski, J.I.,
Nevanlinna, H.,
team of authors (2021) factors. About 50 common
variants have been shown to modify BC risk for mutation carriers. All but three