http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104673891-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6858 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 |
| filingDate | 2014-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2018-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2018-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104673891-B |
| titleOfInvention | A kind of detection method and kit of spinal muscular atrophy associated gene mutation |
| abstract | The present invention relates to the detection method and kit of a kind of spinal muscular atrophy associated gene mutation and its applications.The detection method includes step：The complete genome DNA of extraction detection object；PCR amplification is carried out to IV pair of obtained complete genome DNA to III and PCR primer to II, PCR primer to I, PCR primer using PCR primer, obtains pcr amplification product；Obtained pcr amplification product is analyzed, judges that four sites of the spinal muscular atrophy related gene in sample complete genome DNA to be detected whether there is mutation；The kit include PCR primer to I, PCR primer to II, PCR primer to III and PCR primer to IV；The detection method and kit of the present invention is ingenious in design, and three kinds of genes can be detected while sample is saved, and detects quick, accurate, simplicity, so as to as doctor diagnosed, treatment and the reference frame of medication, suitable for large-scale promotion application. |
| priorityDate | 2014-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 225.