Method for the screening of familial hemiplegic migraine (FHM)
First Claim
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1. Method for screening for familial hemiplegic migraine which comprises searching for the presence of genetic abnormalities via polymorphic analysis linked to familial hemiplegic migraine on the chromosome 19, in the region comprised between the microsatellites D19S216 and D19S215, of a family or of an at risk individual, including fetus.
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Abstract
Method for screening for familial hemiplegic migraine which comprises searching for the presence of a mutated gene responsible for familial hemiplegic migraine on the chromosome 19, in the region comprised between the microsatellites D19S216 and D19S215, of a family or of an at risk individual, including fetus.
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5 Claims
- 1. Method for screening for familial hemiplegic migraine which comprises searching for the presence of genetic abnormalities via polymorphic analysis linked to familial hemiplegic migraine on the chromosome 19, in the region comprised between the microsatellites D19S216 and D19S215, of a family or of an at risk individual, including fetus.
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3. A method for screening for familial hemiplegic migraine which comprises selecting polymorphisms via linkage analysis within microsatellite regions responsible for familial hemiplegic migraine on chromosome 19 with the aid of DNA probes to a linkage analysis with the microsatellites D19S216, D19S76, D19S221, D19S179, D19S226, D19S252, D19S253, D19S244, D19S415, D19S199 and D19S215.
- 4. Method for screening for a subgroup of familial hemiplegic migraine linked to chromosome 19 by a family or an at risk individual, including a fetus, comprising the step of searching for a genetic linkage between DNA polymorphisms and a mutated region linked to the familial hemiplegic migraine, these DNA polymorphisms being located in the region of the chromosome 19 comprised between the microsatellites D19S216 and D19S215, including these microsatellites.
Specification