Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon Ilia and a frameshift in exon XI - Gandrille, S; Vidaud, D; Emmerich, J; Clauser, E; Sie, P; Fiessinger, JN; Alhenc-Gelas, M; Priollet, P; Aiach, M (Br J Haematol, 1991)