Literature DB >> 3600055

[Congenital protein C deficiency in patients with thromboembolic disease. Study of 4 Spanish families].

N Sala, E Muñiz, M Borrell, J Félez, J Fontcuberta.   

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Year:  1987        PMID： 3600055

Source DB:  PubMed          Journal:  Med Clin (Barc)        ISSN： 0025-7753            Impact factor:   1.725


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  1 in total

1.  Acceptor splice site mutation in the invariant AG of intron 5 of the protein C gene, causing type I protein C deficiency.

Authors:  J M Soria; J Fontcuberta; M Chillón; M Borrell; X Estivill; N Sala
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132
  1 in total

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