molecular
genetics methods for confirming the diagnosis of NF1 in the clinic in cases of a combination
Dobrodeeva, V.S.,
Shnayder, N.A.,
Novitsky, M.A.,
Asadullin, A.R.,
Vaiman, E.E.,
Petrova, M.M.,
Limankin, O.V.,
Neznanov, N.G.,
Garganeeva, N.P.,
Nasyrova, R.F. (2022) the significance of
genetic risk factors (carriage of major allele C of SNV rs11100494 of the NPY5R gene