αIIbβ3 variants in ten families with autosomal dominant macrothrombocytopenia: Expanding the mutational and clinical spectrum.

Also, patients from F1-F6 had higher IPF values as compared to patients from F7-F9 (median values: 13% and 9%, respectively), although differences did not reach statistical significance (p>0.05) ( Table 1 ) ( Fig 2J ), maybe because of variability and the low number of cases studied.

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