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Hilbert L., Gaucher C., Fressinaud E., Meyer D., Mazurier C., INSERN network on molecular abnormalities in vWD. A new type 2M ("type B") vWD mutation (G1324A) also at position 561 of the mature vWF subunit. - Throb.Haemost., 1997 (suppl. 2670), p. 654.
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