Bikbova, M.M.,
Usubova, E.L.,
Oganisyana, K.Kh.,
Lobov, S.L.,
Khasanovad, R.R.,
Dzhemilevab, L.U.,
Khusnutdinova, E.K. (2017) to
both hereditary and genetically caused diseases and identified genetic
variants are specific both
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) variants of referral diagnoses of patients with HMSN were identified. They can be divided into 3 subgroups