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?
