Molecular diagnostic of glaucomas associated with chromosomes 1, and method of treatment thereof
CA 2345923 A1 · Owner: Cote, Gilles · Inventors: Raymond, Vincent; Falardeau, Pierre; Anctil, Jean-Louis
Overview
Its claims, description and drawings are in the Canadian Patents Database.
Open the CIPO recordAbstract From the Canadian patent
The present invention relates to the surprising discovery that in an autosomally inherited disease, a homozygote mutant is found to be phenotypically normal and to the uses of such a discovery. The present invention further relates to easy and efficient means to detect mutations in the TIGR/MYOC gene. Further, the present invention relates to methods to diagnose and treat glaucoma or other diseases or conditions in which homoallelic complementation is observed.
Read the whole patent
Listed from its CIPO record in Patent Yard's archive of Canadian patents past their term. Its claims, description and drawings are in the CIPO record and on Google Patents, and the Claude kit works from them.
Why it's free to use
- Filed September 29, 1998. No grant is recorded for it in Canada; had it been granted, its 20-year term would have ended September 29, 2018.
- A certificate of supplementary protection adds at most two years for a drug, so even that would have ended by September 29, 2020.
- We check Canadian rights only. A patent in its family in another country could still be in force: check its family on Google Patents.
Timeline
Timeline From CIPO dates
Sources & verification
Official CIPO records
Everything on this page comes from the CIPO record linked above. Contains information licensed under the Open Government Licence – Canada.