Full Text Available
Note: Clicking the button above will open the full text document at the original institutional repository in a new window.
Variant Spectrum and Genotype–Phenotype Correlations in Iranian Rett Syndrome Patients: Identification of a Novel Frameshift Mutation
Saved in:
| Published in: | Journal of Molecular Neuroscience |
|---|---|
| Format: | Online Article RSS Article |
| Published: |
2026
|
| Subjects: | |
| Tags: |
No Tags, Be the first to tag this record!
|
Similar Items: Variant Spectrum and Genotype–Phenotype Correlations in Iranian Rett Syndrome Patients: Identification of a Novel Frameshift Mutation
- Utilization of Non-pharmacological Interventions in Rett Syndrome: A Systematic Review of the Literature on Supportive Care Management
- Genotype-Phenotype Correlation Analysis of Inherited Variations in Autism Spectrum Disorder Families Identify an Interplay between Sensory Function and Repetitive-behaviour Genes
- SHANK3 Genotype Mediates Speech and Language Phenotypes in a Nonclinical Population
- Adult-Onset Leigh Syndrome due to SURF1 Mutations
- Genetic Spectrum and Phenotypic Variability in Chinese Patients with Multisystem Proteinopathy and Related Disorders
- A Study of the Correlation between VEP and Clinical Severity in Children with Autism Spectrum Disorder