Browsing by Author "Tuzuner, Nukhet"
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Case report of a young patient with transthyretin amyloidosis associated with Gly67Ala mutation
Salihoglu, Ayse; Yildirim, Suleyman; Ar, Muhlis Cem; Hancer, Veysel Sabri; Bozcan, Selma; Yilmaz, Umut; Serin, Nergis; Tuzuner, Nukhet; Celik, Aykut Ferhat (Taylor & Francis Ltd, 2019)Hereditary transthyretin-mediated amyloidosis (hATTR) is a rare, systemic and progressive autosomal dominant disease caused by mutations in the TTR gene. Systemic deposition of amyloidogenic mutant transthyretin results ...