Natural history of 15 patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy.
- DOI
- 10.1186/s13023-026-04348-9
- Published
- 2026 Apr 18
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-026-04348-9,
title = {Natural history of 15 patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy.},
author = {Roberts JP and Tang AF and Hernandez D and Carman B and Oiknine L and Brown C and Hurst S and Tang Y and Urano F},
year = {2026},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-026-04348-9},
url = {https://doi.org/10.1186/s13023-026-04348-9}
}RIS
TY - JOUR TI - Natural history of 15 patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy. AU - Roberts JP AU - Tang AF AU - Hernandez D AU - Carman B AU - Oiknine L AU - Brown C AU - Hurst S AU - Tang Y AU - Urano F PY - 2026 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-026-04348-9 UR - https://doi.org/10.1186/s13023-026-04348-9 ER -
APA
JP, R., AF, T., D, H., B, C., L, O., C, B., S, H., Y, T., & F, U. (2026). Natural history of 15 patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-026-04348-9
Source records
- pubmed · retrieved 2026-09-26T05:21:18.964Z