Polymorphisms in known genes associated with human disease, methods of detection and uses thereof

   
   

The present invention is based on the discovery of novel polymorphisms (SNPs) in the genes known in the art to contribute to human disease. Such polymorphisms can lead to a variety of disorders that are mediated/modulated by a variant human disease associated protein. The present invention provides reagents used for detecting and expressing the variant nucleic acid/protein sequence as well as methods of identifying and using these variants.

 
Web www.patentalert.com

< Transgenic plants that exhibit enhanced nitrogen assimilation

< Agent for treating visual cell function disorder

> Maize nucleic acid encoding a GDP-mannose pyrophosphorylase

> Hypoallergenic transgenic soybeans

~ 00141