Novel mutations relating to x-linked charcot-marie-tooth disease
CA 2270409 A1 · Owner: Sullivan, Charleen M. · Inventors: Sullivan, Charleen M.; Ananth, Uma; Boss, Michael A.
Overview
Its claims, description and drawings are in the Canadian Patents Database.
Open the CIPO recordAbstract From the Canadian patent
Specific mutations in the connexin-32 gene that are associated with X-linked Charcot-Marie-Tooth (CMT) disease are disclosed. Methods of diagnosing, X-linked CMT disease are also disclosed. Methods include hybridization analysis, such as Southern or Northern analysis which use hybridization of mutant , connexin-32 nucleic acid probes to connexin-32 genes; direct mutation analysis by restriction, digest; sequencing of the connexin-32 gene; hybridization of an allelespecific, oligonucleotide with genomic DNA; or identification of mutant connexin-32 proteins. Mutant connexin-32 nucleic acid probes are also disclosed. The mutant, connexin-32 nucleic acid probes have a mutation in at least …
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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 May 12, 1999. No grant is recorded for it in Canada; had it been granted, its 20-year term would have ended May 12, 2019.
- A certificate of supplementary protection adds at most two years for a drug, so even that would have ended by May 12, 2021.
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Official CIPO records
Everything on this page comes from the CIPO record linked above. Contains information licensed under the Open Government Licence – Canada.