Next Generation Mendelian Genetics: Hereditary Neurological Disorders

The NHGRI Next Generation Mendelian Genetics project uses exome resequencing to identify variants in unsolved Mendelian diseases.

This dataset was obtained from exome analyses of people with hereditary neurologic disorders of unknown cause.

• Type: Case Set
• Archiver: The database of Genotypes and Phenotypes (dbGaP)