is diagnosed in 5 % of children with NF1, accounting for 80 % of all cases of this
pathology in the general
Роль мутаций в гене NF1 в спорадическом канцерогенезеThe review article presents data on
somatic inactivation of NF1 gene as a cause of sporadic
, and the development of age-associated
pathologies. Transposons are capable of translocating into strictly defined loci
consolidation. The cause of aging and neurodegenerative diseases with memory impairment is the
pathological-inflammatory macrophage phenotype, which contributes to
pathological immune response, foam cell formation