Literature DB >> 9459358

A new (K1518E) candidate mutation detected by universal heteroduplex generator analysis in a patient with type 2A (phenotype IIA) von Willebrand disease.

M S Enayat, B D Theophilus, F G Hill, P E Rose, D Culpan, J Bidwell, G R Standen.   

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Year:  1998        PMID: 9459358

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


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  1 in total

Review 1.  Molecular genetics of type 2 von Willebrand disease.

Authors:  Edith Fressinaud; Claudine Mazurier; Dominique Meyer
Journal:  Int J Hematol       Date:  2002-01       Impact factor: 2.490

  1 in total

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