# Editorial for the special collection: frontiers in rare disease genetics

**Authors:** Murim Choi

PMC · DOI: 10.1186/s44342-025-00039-2 · Genomics & Informatics · 2025-03-07

## Full-text entities

- **Diseases:** spinal muscular atrophy (MESH:D009134), sensory disorder (MESH:D012678), neurological diseases (MESH:D020271), rare (MESH:D035583), sensorineural hearing loss (MESH:D006319), age-related hearing loss (MESH:D010024), NMDs (MESH:D009468), Duchenne muscular dystrophy (MESH:D020388)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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Source: https://tomesphere.com/paper/PMC11887329