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Autor:
Yasemin Isik Balci, Dolunay Gürses, Serap Semiz, Tamer Özsari, Kazım Küçüktaşçı, Mustafa Saçar, Ender Semiz, Gökhan Önem, Füsun Düzcan, Doğangün Yüksel
Wolfram syndrome-1 is a rare and severe autosomal recessive neurodegenerative disease characterized by diabetes mellitus (DM), optic atrophy, diabetes insipidus, and deafness. Poorly controlled type 1 DM increases the risk for thrombosis. However, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab2cccfd03e5214223a17b678f87f590
https://hdl.handle.net/11499/9422
https://hdl.handle.net/11499/9422