Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency

Publisher: John Wiley & Sons Inc

E-ISSN: 1365-2362|14-2972|10|1087-1091

ISSN: 0014-2972

Source: EUROPEAN JOURNAL OF CLINICAL INVESTIGATION (ELECTRONIC), Vol.14-2972, Iss.10, 2015-10, pp. : 1087-1091

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Abstract