http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006158349-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_72c063ef3226e3385e017f9a72feaee7 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 |
| filingDate | 2004-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a38f7d4438209ea514c0ca98bdad307 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4eb045b31b6c774297652dbe352046db http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bde819fad321313ba6b24980abf31c85 |
| publicationDate | 2006-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2006158349-A |
| titleOfInvention | Methods for detecting genetic mutations that regulate hearing loss |
| abstract | To find a new gene related to hearing loss and to establish a screening means for hearing loss (congenital hearing loss or acquired progressive hearing loss) using the gene. [MEANS FOR SOLVING PROBLEMS] The presence of congenital deafness or acquired progressive deafness due to mutations in human VEST1 gene and human COL9A1 gene, which is a gene having a function not directly related to deafness, and mutations in these genes Is detected to detect deafness (congenital deafness or acquired progressive deafness) at the gene level, and a mutation in one or both of the human VEST1 gene and the human COL9A1 gene is detected. It has been found that the above problem can be solved by providing a gene detection method for detecting hearing loss. [Selection figure] None |
| priorityDate | 2004-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 236.