Phenotype/Genotype Correlations in Movement Disorders
Phenotype/Genotype Correlations in Movement Disorders
Recruiting · NCT00018889 · Registry updated 2026-10-02Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Phenotype/Genotype Correlations in Movement Disorders | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Spinocerebellar Degenerations, brain disorder, central nervous system disorder, cerebellar disorder, essential tremor, hereditary disease, inherited neurodegenerative disorder, movement disorder, nervous system disorder, neurodegenerative disease, spinal cord disorder | Recruiting | Not stated | 2026-10-02 | NCT00018889 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| National Institute of Neurological Disorders and Stroke (NINDS) | 370 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| National Institutes of Health Clinical Center | Bethesda | United States | 800 |