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INDIRECT GENOTYPIC METHOD FOR DIAGNOSING TYPE 2 FAMILIAL HEMIPLEGIC MIGRAINE
INDIRECT GENOTYPIC METHOD FOR DIAGNOSING TYPE 2 FAMILIAL HEMIPLEGIC MIGRAINE
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机译:间接基因型方法诊断2型家族性偏头痛
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摘要
the present invention relates to a method for diagnosis of indirect genotypethe type 2 family hemiplegic migraine in an individual, whichin that, we highlighted in the dna of the individual in the presence of aa marker located on the chromosome in the locus 1q21 - however limited by thed1s2343 d1s2844 markers and the marker is associated with the occurrence of thehemipalegic migraine family within the family.
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