http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106755335-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6858 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6858 |
| filingDate | 2016-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2020-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2020-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-106755335-B |
| titleOfInvention | Detection primer, kit and detection method for gene mutation of Leber hereditary optic neuropathy mitochondria DNA |
| abstract | The invention relates to a detection primer, a kit and a detection method for gene mutation of Leber hereditary optic neuropathy mitochondria. The method is based on the Sanger sequencing principle, has the characteristics of high sensitivity, stability and accuracy, can be used for simultaneously detecting the four most common pathogenic mutations of LHON mtDNA, solves the problems of low sensitivity, insufficient specificity, easiness in pollution, high cost and the like of the conventional method for detecting LHON mitochondrial DNA mutation, provides an accurate gene diagnosis method for LHON, and has important significance for genetic consultation and gene therapy of the disease. |
| priorityDate | 2016-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 21.