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Method of the diagnostic genotypic indirect migraine hemiplegic treatment of type 2
Method of the diagnostic genotypic indirect migraine hemiplegic treatment of type 2
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机译:诊断型2型间接偏头痛偏瘫的治疗方法
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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.
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