Browsing by Subject "CXCL12"

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  • Karaosmanoglu, Beren; Kocaefe, Çetin Y.; Söylemezoğlu, Figen; Anlar, Banu; Varan, Ali; Vargel, İbrahim; Ayter, Şükriye (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 ...