Now showing items 1-2 of 2
Heightened CXCR4 and CXCL12 expression in NF1-associated neurofibromas
(Springer Berlin Heidelberg, 2018-05-01)
Neurofibromatosis type 1 (NF1) is the most common neurogenetic disorder worldwide, and its clinical presentations are highly variable. NF1 is caused by mutations in the NF1 gene, and 50% of NF1 cases are sporadic, which ...
Clinical findings and mutation analysis of NF1 patients in Turkey
(Elsevier B.V., 2018-02)
Neurofibromatosis type 1 (NF1) is an autosomal dominant disease that is caused by mutations of the NF1 gene. NF1 is clinically characterized by neurofibromas, pigmentation anomalies, and an increased risk of malignant ...