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Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease
Authors:Gallinaro Lisa  Sartorello Francesca  Pontara Elena  Cattini Maria Grazia  Bertomoro Antonella  Bartoloni Lucia  Pagnan Antonio  Casonato Alessandra
Affiliation:Department of Medical and Surgical Sciences, University of Padua Medical School, secondchairof internal Medicine, Padua, Italy.
Abstract:
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