Yanchao, L.,
Sibin, Z.,
Gareev, I.,
Huan, X.,
Junfei, Z.,
Chunyang, L.,
Beylerli, O.,
Sufianov, A.,
Chao, Y.,
Yuyan, G.,
Xun, X.,
Ahmad, A. (2022) patients, to clarify the common
genes of both, and to identify common pathways and potential drugs
», «treatment», «frequency», «prevalence», «genotype-phenotype correlation», « modifier
genes». Results
by specific mutations in the NF1
gene (causing substitutions of amino acids in neurofibromin: p.Arg1038, p