Method for the diagnosis of familial hemiplegic migraine (fhm)

C - Chemistry – Metallurgy – 12 – Q

Patent

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C12Q 1/68 (2006.01)

Patent

CA 2116633

The invention relates to method for the genotype diagnosis of FHM, by searching the presence of a mutated gene responsible for the disease, comprising the search of the presence of a mutation responsible for FHM on the chromosome 19, in the region of it comprised between the microsatellites D19S216 and D19S215, of a family or of an at risk individual, including foetus.

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