Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia
Recruiting · NCT06999096 · Registry updated 2026-05-20Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia | Dyskinesias, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, central nervous system disorder, combined dystonia, dystonic disorder, movement disorder, nervous system disorder | Recruiting | Not applicable | 2026-05-20 | NCT06999096 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| University Hospital, Strasbourg, France | 263 |
4 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| CHRU Nancy | Nancy | France | 8 |
| CHU de Montpellier - Hôpital Gui de Chauliac | Montpellier | France | 2 |
| Hôpital Pitié Salpêtrière- APHP | Paris | France | 1 |
| Hôpitaux Universitaires de Strasbourg | Strasbourg | France | 18 |