Expanding the genetic spectrum of neurogenetic disorders in moroccan families by exome sequencing: identification of candidate variants in RYR3, POLR3A, and LAMA2
- DOI
- 10.1007/s11033-026-11900-0
- Published
- 2026-05-11
- Container
- Molecular Biology Reports
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1007/s11033-026-11900-0,
title = {Expanding the genetic spectrum of neurogenetic disorders in moroccan families by exome sequencing: identification of candidate variants in RYR3, POLR3A, and LAMA2},
author = {Fatima Ezzahra Chentoufi and Assia Idyahia and Madoussou Toure and Adil El Hamouchi and Abdelhamid Barakat and Houda Benrahma and Hicham Charoute},
year = {2026},
journal = {Molecular Biology Reports},
doi = {10.1007/s11033-026-11900-0},
url = {https://doi.org/10.1007/s11033-026-11900-0}
}RIS
TY - JOUR TI - Expanding the genetic spectrum of neurogenetic disorders in moroccan families by exome sequencing: identification of candidate variants in RYR3, POLR3A, and LAMA2 AU - Fatima Ezzahra Chentoufi AU - Assia Idyahia AU - Madoussou Toure AU - Adil El Hamouchi AU - Abdelhamid Barakat AU - Houda Benrahma AU - Hicham Charoute PY - 2026 JO - Molecular Biology Reports DO - 10.1007/s11033-026-11900-0 UR - https://doi.org/10.1007/s11033-026-11900-0 ER -
APA
Chentoufi, F. E., Idyahia, A., Toure, M., Hamouchi, A. E., Barakat, A., Benrahma, H., & Charoute, H. (2026). Expanding the genetic spectrum of neurogenetic disorders in moroccan families by exome sequencing: identification of candidate variants in RYR3, POLR3A, and LAMA2. Molecular Biology Reports. https://doi.org/10.1007/s11033-026-11900-0
Source records
- crossref · retrieved 2026-09-26T18:44:52.761Z