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Method of the diagnostic genotypic indirect migraine hemiplegic treatment of type 2

机译:诊断型2型间接偏头痛偏瘫的治疗方法

摘要

The invention concerns an indirect genotypic method for diagnosing type 2 familial hemiplegic migraine in a person, characterised in that it consists in: isolating in said person's DNA the presence of a marker located on the 1a21-q23 chromosome in the locus limited by the D1S2343 and D1S2844 markers, said marker being related with the occurrence of familial hemiplegic migraine in his family.
机译:本发明涉及一种用于诊断人的2型家族性偏瘫偏头痛的间接基因型方法,其特征在于:在所述人的DNA中分离位于由D1S2343限制的基因座中的1a21-q23染色体上的标志物的存在。 D1S2844标志物,该标志物与他家中家族性偏瘫性偏头痛的发生有关。

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