How Studying Rare Disease Leads to Mechanistic Insights and Therapeutic Development: Lessons from Nonmammalian Models
- DOI
- 10.1146/annurev-genom-020525-025811
- Published
- 2026-08-25
- Container
- Annual Review of Genomics and Human Genetics
- Publisher
- Annual Reviews
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1146/annurev-genom-020525-025811,
title = {How Studying Rare Disease Leads to Mechanistic Insights and Therapeutic Development: Lessons from Nonmammalian Models},
author = {Paige Hall and Michael Wangler and Jonathan Andrews},
year = {2026},
journal = {Annual Review of Genomics and Human Genetics},
doi = {10.1146/annurev-genom-020525-025811},
url = {https://doi.org/10.1146/annurev-genom-020525-025811}
}RIS
TY - JOUR TI - How Studying Rare Disease Leads to Mechanistic Insights and Therapeutic Development: Lessons from Nonmammalian Models AU - Paige Hall AU - Michael Wangler AU - Jonathan Andrews PY - 2026 JO - Annual Review of Genomics and Human Genetics DO - 10.1146/annurev-genom-020525-025811 UR - https://doi.org/10.1146/annurev-genom-020525-025811 ER -
APA
Hall, P., Wangler, M., & Andrews, J. (2026). How Studying Rare Disease Leads to Mechanistic Insights and Therapeutic Development: Lessons from Nonmammalian Models. Annual Review of Genomics and Human Genetics. https://doi.org/10.1146/annurev-genom-020525-025811
Source records
- crossref · retrieved 2026-09-26T11:52:31.740Z