Asper Neurogenetics


Amyotrophic Lateral Sclerosis
Autism Spectrum Disorders
Brunner Syndrome
Charcot-Marie-Tooth Disease
Congenital Myasthenic Syndrome
Congenital Myopathy and Distal Myopathy
Cornelia de Lange Syndrome
Fragile X Syndrome
Frontotemporal Dementia
Hereditary Spastic Paraplegia
Joubert Syndrome
Leukodystrophy and Leukoencephalopathy
Limb-Girdle Muscular Dystrophy
Menkes Disease
Mitochondrial Diseases
Neurodegeneration with Brain Iron Accumulation
Parkinson’s Disease
Smith-Lemli-Opitz Syndrome
Spinocerebellar Ataxia
Tuberous Sclerosis
Wilson Disease
Whole Exome Sequencing

EMQN Certificate of Participation

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.