Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2

por Cenedese, Valentina, Mezzavilla, Massimo, Morgan, Anna, Marino, Renato, Ettorre, Cosimo Pietro, Margaglione, Maurizio, Gasparini, Paolo, Menini, Anna
Publicado 2015