# Interest of High-throughput Sequencing of RNAs for the Diagnosis of Heterogeneous Genetic Diseases

> **NCT03971292** · — · UNKNOWN · sponsor: **University Hospital, Strasbourg, France** · enrollment: 15 (estimated)

## Conditions studied

- DNA Sequencing
- Diagnosis of Genetic Diseases of Heterogeneous Origin

## Interventions

- **GENETIC:** RNA sequencing

## Key facts

- **NCT ID:** NCT03971292
- **Lead sponsor:** University Hospital, Strasbourg, France
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2019-06
- **Primary completion:** 2019-07
- **Final completion:** 2022-07
- **Target enrollment:** 15 (ESTIMATED)
- **Last updated:** 2019-06-03


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03971292

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03971292, "Interest of High-throughput Sequencing of RNAs for the Diagnosis of Heterogeneous Genetic Diseases". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT03971292. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*