http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113151419-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/C12Q1-6858 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 |
| filingDate | 2021-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2022-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-113151419-B |
| titleOfInvention | Spinal muscular atrophy test |
| abstract | The invention discloses a spinal muscular atrophy detection method, wherein the spinal muscular atrophy detection method comprises the extraction of sample genomic DNA, the design and synthesis of amplification primers and detection probes, fluorescence quantitative PCR reaction, the relative copy number of genes Calculation and analysis of base mutation levels. The spinal muscular atrophy detection method of the invention can realize the simultaneous detection of the relative copy number of SMN1, the relative copy number of SMN2 and the point mutation of SMN1, the detection is comprehensive, the steps are simple, and the clinical application and popularization are easy. |
| priorityDate | 2021-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 42.