Browsing by Author Lejla Shabani-Misini

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Point mutation C18R in pre-pro-PTH gene in brother and sister with hypoparathyroidism, Fahr’s syndrome and epilepsyPlasheski, Tosho ; Lejla Shabani-Misini; Iskra Bitoska ; Sasha Jovanovska Mishevska ; Biljana Todorova; Atanas Sivevski ; Antonio Georgiev ; Dijana Plashevska-Karanfilska2021Article