Abstract: The present invention pertains to the domain of brain diseases, and provides novel markers and methods for diagnosing a brain alteration in an individual, especially in patients suffering from neurodegenerative diseases such as Alzheimer's disease. The present invention also provides tools for evaluating the probability, for an individual, of developing the disease, as well as a target for identifying new drugs for treating neurodegenerative diseases such as Alzheimer's disease. In particular, the invention provides a genetic marker based on combination of two single nucleotide polymorphism, at positions ?389 and ?241 of the ornithine transcarbamylase (OTC) gene.
Type:
Grant
Filed:
April 18, 2007
Date of Patent:
February 14, 2012
Assignees:
Genoscreen, Institut National de la Sante et de la Recherche Medicale (INSERM)
Inventors:
Philippe Amouyel, Jean-Charles Lambert, Stéphanie Ferreira
Abstract: The present invention pertains to the domain of brain diseases, and provides novel markers and methods for diagnosing a brain alteration in an individual, especially in patients suffering from neurodegenerative diseases such as Alzheimer's disease. The present invention also provides tools for evaluating the probability, for an individual, of developing the disease, as well as a target for identifying new drugs for treating neurodegenerative diseases such as Alzheimer's disease. In particular, the invention provides a genetic marker based on combination of two single nucleotide polymorphism, at positions ?389 and ?241 of the ornithine transcarbamylase (OTC) gene.
Type:
Application
Filed:
April 18, 2007
Publication date:
July 9, 2009
Applicant:
Genoscreen
Inventors:
Philippe Amouyel, Jean-Charles Lambert, Stéphanie Ferreira