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  4. A novel mutation in gp1bb reveals the role of the cytoplasmic domain of gpibß in the pathophysiology of bernard¿soulier syndrome and gpib¿ix complex assembly
 
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A novel mutation in gp1bb reveals the role of the cytoplasmic domain of gpibß in the pathophysiology of bernard¿soulier syndrome and gpib¿ix complex assembly

Journal
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
ISSN
1661-6596
Author(s)
Barozzi S.
Bozzi V.
De Rocco Daniela 
Giangregorio T.
Noris P.
Savoia Anna 
Pecci A.
DOI
10.3390/ijms221910190
Project(s)
Applicazione della piattaforma Ion Torrent per la diagnosi molecolare delle piastrinopenie ereditarie 
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C.A.R.S.O. - I.R.C.C.S. materno infantile Burlo Garofolo

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