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ITA
Home
About us
Eurofins Genoma
Our Team
Quality/Accreditation
Funded Projects
Job Opportunities
Specialized Areas
Useful information
What is a genetic test
Where you can test
How to request the test
How the genetic test is performed
Sample collection and management
Storage and shipment of biological samples
Forms
Online Reports
Contacts
ENG
ITA
Category:
Neurology
RETT Syndrome
Spinocerebellar Ataxia Type 3
Tay Sachs (HEXA) Disease – Most Mutations
CYP2D6
CYP1A2
CYP2C9
Hereditary Spastic Paraplegia – Panel
Myotonic Dystrophy Type 2
Galactosemia – Most Mutations
Spinocerebellar Ataxia Type 2
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