Paar, V.,
Jirak, P.,
Larbig, R.,
Zagidullin, N.S.,
Brandt, M.C.,
Lichtenauer, M.,
Hoppe, U.C.,
Motloch, L.J. (2019) of Ca2+-handling in the development of congenital as well as acquired ventricular arrhythmia
syndromesSolovyev, A.V.,
Barashkov, N.A.,
Bady-Khoo, M.S.,
Zytsar, M.V.,
Posukh, O.L.,
Romanov, G.P.,
Rafailov, A.M.,
Sazonov, N.N.,
Alexeev, A.N.,
Dzhemileva, L.U.,
Khusnutdinova, E.K.,
Fedorova, S.A. (2017) -q12) associated with congenital non-
syndromic autosomal recessive deafness. This mutation
AKHMADIEV, N.S.,
AKHMETOVA, V.R.,
IBRAGIMOV, A.G.,
GALIMOVA, A.M.,
GALIMOVA, R.A.,
AGLETDINOV, E.F.,
KATAEV, V.A.,
KHAIRULLINA, V.R. (2019) of the cytolytic
syndrome, the liver excretory function, carbohydrate, protein and lipid metabolism