Asper Neurogenetics

Asper Neurogenetics includes genetic tests for the diagnostics of diseases with neurologic and metabolic involvement.

Diseases involved in the testing portfolio are genetically and phenotypically heterogeneous group of severe disorders such as inherited neuropathies and mitochondrial diseases. For the diagnostics of diseases with an overlapping spectrum of phenotypes, we offer a comprehensive variety of tests with different testing strategies.

 

Pricing

 

Charcot-Marie-Tooth Disease
Cornelia de Lange Syndrome
Craniosynostosis
Dystonia
Fragile X Syndrome
Frontotemporal Dementia
Epilepsy
Hereditary Spastic Paraplegia
Joubert Syndrome
Menkes Disease
Microcephaly
Mitochondrial Diseases
Neurodegeneration with Brain Iron Accumulation
Parkinson Disease
Smith-Lemli-Opitz Syndrome
Spinocerebellar Ataxia
Wilson Disease
Whole Exome Sequencing