MECP2 Variant Spectrum and Genotype-Phenotype Correlations in Iranian Rett Syndrome Patients: Identification of a Novel Frameshift Mutation.
- DOI
- 10.1007/s12031-026-02545-6
- Published
- 2026 May 29
- Container
- Journal of molecular neuroscience : MN
- Publisher
- Not recorded
- Open access
- no
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Cite this work
BibTeX
@article{allodium:10.1007/s12031-026-02545-6,
title = {MECP2 Variant Spectrum and Genotype-Phenotype Correlations in Iranian Rett Syndrome Patients: Identification of a Novel Frameshift Mutation.},
author = {Booalizadeh P and Salahshourifar I and Rabbani B and Rezvani M and Ashrafi MR and Mahdieh N},
year = {2026},
journal = {Journal of molecular neuroscience : MN},
doi = {10.1007/s12031-026-02545-6},
url = {https://doi.org/10.1007/s12031-026-02545-6}
}RIS
TY - JOUR TI - MECP2 Variant Spectrum and Genotype-Phenotype Correlations in Iranian Rett Syndrome Patients: Identification of a Novel Frameshift Mutation. AU - Booalizadeh P AU - Salahshourifar I AU - Rabbani B AU - Rezvani M AU - Ashrafi MR AU - Mahdieh N PY - 2026 JO - Journal of molecular neuroscience : MN DO - 10.1007/s12031-026-02545-6 UR - https://doi.org/10.1007/s12031-026-02545-6 ER -
APA
P, B., I, S., B, R., M, R., MR, A., & N, M. (2026). MECP2 Variant Spectrum and Genotype-Phenotype Correlations in Iranian Rett Syndrome Patients: Identification of a Novel Frameshift Mutation.. Journal of molecular neuroscience : MN. https://doi.org/10.1007/s12031-026-02545-6
Source records
- pubmed · retrieved 2026-09-26T08:03:44.721Z
- europe-pmc · retrieved 2026-09-26T08:03:44.749Z