Bikbova, M.M.,
Usubova, E.L.,
Oganisyana, K.Kh.,
Lobov, S.L.,
Khasanovad, R.R.,
Dzhemilevab, L.U.,
Khusnutdinova, E.K. (2017)
development is widely recognized. To date, a large number of candidate
genes have been investigated
Сайфуллина, Е.В.,
Магжанов, Р.В.,
Хидиятова, И.М.,
Хуснутдинова, Э.К.,
Saifullina, E.V.,
Magzhanov, R.V.,
Khidiiatova, I.M.,
Khusnutdinova, E.K. (2017) genetically heterogenous and clinically
polymorphic group of diseases which predominantly affect peripheral
Khusnutdinova, E.K.,
Dzhemileva, L.U.,
Lobov, S.L.,
Kuznetzov, D.U.,
Nazirova, A.G.,
Nurgalina, E.M.,
Barashkov, N.A.,
Fedorova, S.A. (2017) carrier frequency of c.35delG,
c.167delT and c.235delC mutations of the GJB2
gene in 17 populations
-sensory neuropathies caused by mutations in the GJB1
gene (gap junction B1 type). The authors have established earlier