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INDIRECT GENOTYPIC METHOD FOR DIAGNOSING TYPE 2 FAMILIAL HEMIPLEGIC MIGRAINE

机译:间接基因型方法诊断2型家族性偏头痛

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.
机译:本发明涉及一种间接基因型的诊断方法个人的2型家庭偏瘫偏头痛在这一点上,我们在个人的dna中突出显示了位于基因座1q21的染色体上的标记-但受d1s2343标记和d1s2844标记与发生偏头痛家庭内有偏头痛。

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