Gray platelet syndrome: Novel mutations of the NBEAL2 gene.

BOTTEGA R; NICCHIA E; ALFANO C.; GLEMBOTSKY AC.; PASTORE A.; BERTAGGIA-CALDERARA D; BISIG B; DUCHOSAL MA; ARBESÚ G; ALBERIO L; HELLER PG.; SAVOIA A.

AMERICAN JOURNAL OF HEMATOLOGY

WILEY-LISS, DIV JOHN WILEY & SONS INC

Lugar: New York; Año: 2017

0361-8609

ROBERTA BOTTEGA1, ELENA NICCHIA2, CATERINA ALFANO3, ANA C. GLEMBOTSKY4,ANNALISA PASTORE3, DEBORA BERTAGGIA-CALDERARA5, BETTINA BISIG6,MICHEL A. DUCHOSAL5, GUILLERMO ARBESU´ 7, LORENZO ALBERIO5, PAULA G. HELLER4,ANNA SAVOIA1,21Department of Medical Sciences, University of Trieste, Italy 2Institute for Maternal and Child Health ? IRCCS Burlo Garofolo, Trieste, Italy 3Maurice Wohl Institute, King?s College London, UK 4Instituto de Investigaciones Medicas Alfredo Lanari, Universidad de Buenos Aires,CONICET, Buenos Aires, Argentina 5Service and Central Laboratory of Hematology, University Hospital of Lausanne (CHUV),Switzerland 6Institute of Pathology, CHUV University Hospital and University of Lausanne, Switzerland7Hospital Pediatrico Dr. Humberto Notti, Mendoza, ArgentinaAdditional Supporting Information may be found in the online version of this article.Conflict of interest: Nothing to report.Funding information Italian Ministry of Health, Grant/Award Number: RF-2010-2309222;Telethon Foundation, Grant/Award Number: GGP13082; IRCCS Burlo Garofolo (RicercaCorrente); Cariplo Foundation, Grant/Award Number: 2012-0529