Literature DB >> 18852482

True congenital prothrombin deficiency due to a 'new' mutation in the pre-propeptide (ARG-39 GLN).

A Girolami1, L Santarossa, P Scarparo, N Candeo, B Girolami.   

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Year:  2008        PMID： 18852482     DOI： 10.1159/000162281

Source DB:  PubMed          Journal:  Acta Haematol        ISSN： 0001-5792            Impact factor:   2.195


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  1 in total

1.  A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene.

Authors:  Eman M Mansory; Pratibha Bhai; Alan Stuart; Lori Laudenbach; Bekim Sadikovic; Alejandro Lazo-Langner
Journal:  Res Pract Thromb Haemost       Date:  2021-05-03
  1 in total

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