Ara
Toplam kayıt 2, listelenen: 1-2
Investigation of genetic variations of IL17 for vitiligo disease
(Kuwait Medical Assoc, 2019)
Objective: Vitiligo is a disorder of pigmentation characterized by the presence of depigmented skin macules due to a chronic and progressive loss of melanocytes from the cutaneous epidermis. Among many different etiologic ...
The effect of FOXO gene family variants and global DNA methylation on RRMS disease
(Wiley, 2019)
5th Congress of the European-Academy-of-Neurology