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] Filtri: First Letter Of Last Name è P and Autore is Pecci, A [Clear All Filters]
. R705H mutation of MYH9 is associated with MYH9-related disease and not only with non-syndromic deafness DFNA17. Clin Genet 2015;88(1):85-9.
. International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country. J Thromb Haemost 2012;10(8):1653-61.