diagnosis of AVNFH in individuals who are at greater risk for the
disease. © Volkov E.E., Goloshchapov A
Роль мутаций в гене NF1 в спорадическом канцерогенезе. Prospects for gene therapy of these
diseases are considered. © 2021 Uspehi Molekularnoj Onkologii. All
with microdeletions are characterized by more severe
disease symptoms (more often facial dysmorphism, skeletal
Mustafin, R.N.,
Bermisheva, M.A.,
Karunas, A.S.,
Akhmetshin, A.A.,
Monakhova, A.S.,
Khusnutdinova, E.K. (2025) the
disease. Materials and methods: clinical and epidemiological study of NF1 patients in the Republic
Функциональный дуализм транскриптов транспозонов в эволюции геномов эукариот. This substantiates the associations of multifactorial
diseases with the gene SNP since they can cause inactivation
Изменения иммунной системы в патогенезе нейрофиброматоза 1-го типа the oncosuppressor neurofibromin. The
disease has a specific progressive course with multiple neurofibromas