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Waluta


Genetic Testing Offered by NZOZ Genomed

Progressive myoclonic epilepsy
 Test code: CSTB-1

Progressive myoclonic epilepsy (EPM1), Unverricht-Lundborg disease (ULD).
Identification of an expansion of the (CCCCGCCCCGCG)n motif repeat in the CSTB gene. This expansion  represents the most common genetic cause of EPM1 (90% alleles)

Processing Time: Time: up to 8 weeks

Price:  990.00 zł
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We perform genetic testing from:

Ikona opcji  venous blood collected

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