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classificationCPCInventive 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/C12Q1-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-12
filingDate 1998-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5adccf3b8600d6b0718a1d7b4d4e99dd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82db8f9cb6b2c9170e9764017a1162b4
publicationDate 1998-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2292795-A1
titleOfInvention Indirect genotypic method for diagnosing type 2 familial hemiplegic migraine
abstract The present invention relates to a method of indirect genotypic diagnosis familial hemiplegic migraine type 2 in an individual, characterized in that: it highlights in the DNA of said individual the presence of a marker located on chromosome 1q21-q23 in the locus bounded by markers D1S2343 and D1S2844, said marker being linked to the occurrence of familial hemiplegic migraine within the family.
priorityDate 1997-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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