Machine-Readable Database for Genotype-Phenotype Analyses in Rare Diseases Using FKTN-related Congenital Muscular Dystrophies as a Prototype.
- DOI
- 10.21203/rs.3.rs-10856264/v1
- Published
- 2026 Sep 17
- Container
- Research square
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.21203/rs.3.rs-10856264/v1,
title = {Machine-Readable Database for Genotype-Phenotype Analyses in Rare Diseases Using FKTN-related Congenital Muscular Dystrophies as a Prototype.},
author = {Lefkowitz ME and Eisenberg SG and Huang R and Mudunuri US and Leaman R and Lu Z and Gorokhova S and Haugabook SJ and Ottinger EA and Knebel AR and Lo DC and Bönnemann CG and Foley AR},
year = {2026},
journal = {Research square},
doi = {10.21203/rs.3.rs-10856264/v1},
url = {https://doi.org/10.21203/rs.3.rs-10856264/v1}
}RIS
TY - JOUR TI - Machine-Readable Database for Genotype-Phenotype Analyses in Rare Diseases Using FKTN-related Congenital Muscular Dystrophies as a Prototype. AU - Lefkowitz ME AU - Eisenberg SG AU - Huang R AU - Mudunuri US AU - Leaman R AU - Lu Z AU - Gorokhova S AU - Haugabook SJ AU - Ottinger EA AU - Knebel AR AU - Lo DC AU - Bönnemann CG AU - Foley AR PY - 2026 JO - Research square DO - 10.21203/rs.3.rs-10856264/v1 UR - https://doi.org/10.21203/rs.3.rs-10856264/v1 ER -
APA
ME, L., SG, E., R, H., US, M., R, L., Z, L., S, G., SJ, H., EA, O., AR, K., DC, L., CG, B., & AR, F. (2026). Machine-Readable Database for Genotype-Phenotype Analyses in Rare Diseases Using FKTN-related Congenital Muscular Dystrophies as a Prototype.. Research square. https://doi.org/10.21203/rs.3.rs-10856264/v1
Source records
- pubmed · retrieved 2026-09-26T05:47:58.454Z
- europe-pmc · retrieved 2026-09-26T05:47:58.468Z