Mustafin, R.N.,
Bermisheva, M.A.,
Karunas, A.S.,
Akhmetshin, A.A.,
Monakhova, A.S.,
Khusnutdinova, E.K. (2025) of the genetic causes of NF1 can become the basis for prenatal diagnosis and the use of new
methods of treating
Mukhametov, U.F.,
Lyulin, S.V.,
Borzunov, D.Y.,
Gareev, I.F.,
Beylerli, O.A.,
Sufianov, A.A. (2022) as the possibilities of preventing and treating the HO process. Materials and
methods PubMed, Embase, the Cochrane
methods for NF1 mutations in NF1 families for prenatal prophylaxis. Mutations in NF1 gene play roles