Study

Next Generation Mendelian Genetics: Hereditary Neurological Disorders

Study ID Alternative Stable ID Type
phs000707 Case Set

Study Description

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.

Archive Link Archive Accession
dbGaP phs000707

Who archives the data?

There are no publications available