Association of htra1 mutations and familial ischemic...

Details Association of htra1 mutations and familial ischemic... Association of htra1 mutations and familial ischemic...

C - Chemistry, Metallurgy

12

N

C12N 15/00 (2006.01) A61K 48/00 (2006.01) A61P 43/00 (2006.01) C12Q 1/68 (2006.01)

Patent

CA 2759457

The present invention provides a method of diagnosing a cerebrovascular disease in a human comprising the steps of: (a) measuring a mutation of HTRA1 gene in a test sample from said human; and (b) determining if the mutation of HTRA1 gene in said test sample correlates with a cerebrovascular disease in said human.

La présente invention porte sur un procédé de diagnostic d'une maladie cérébrovasculaire chez un être humain comprenant les étapes consistant à : (a) mesurer une mutation du gène HTRA1 dans un échantillon de test provenant dudit être humain ; et (d) déterminer si la mutation du gène HTRA1 dans ledit échantillon de test est corrélée à une maladie cérébrovasculaire chez ledit être humain.

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