Author

Zahra Shahbazi

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Open access Jan 2026

Whole‐Exome Sequencing in Undiagnosed Muscular Dystrophies: A High Diagnostic Yield and Novel Insights From Iranian Families

This study expands the mutational spectrum of MDs in Iran and provides critical data for genetic counseling, prenatal diagnosis, and future therapeutic development, and underscores the importance of population‐specific genomic studies.

Nasibeh Soltani, Zahra Shahbazi, M. Fallah et al. · Human Mutation · 0 citations