New research shows that while a three-base pair, in-frame deletion called p.Met992del in the NF1 gene has a mild phenotype for people with the genetic disorder neurofibromatosis type 1, or NF1, the ...
Overall, the current study represents a comprehensive evaluation of an important patient cohort. Continued efforts to understand the factors that influence LFS phenotype, the interaction between these ...
The following represents disclosure information provided by authors of this manuscript. All relationships are considered compensated. Relationships are self-held unless noted. I = Immediate Family ...
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