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J Mol Neurosci ; 51(2): 425-7, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23765175

ABSTRACT

The mutation FV Leiden (G1691A) is the most common mutation worldwide with a variable allelic frequency between countries. More frequent in the European and Caucasian populations and rare or absent in African native population, the FVL was studied in the Moroccan population (They-They et al. Ann Hum Biol 37(6):767-777, 2010) and is totally absent as reported previously by (Mathonnet et al. Thromb Haemost 88(6):1073-1074, 2002). Here, another mutation in FV (Q773Term) was detected in a Moroccan patient, which took our interest for this study and establishes the first epidemiological database for future associated studies concerning neurovascular diseases.


Subject(s)
Codon, Nonsense , Factor V/genetics , Gene Frequency , Population/genetics , Adult , Arabs/genetics , Female , Humans , Male , Middle Aged , Morocco
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