Items where Author is "Ali, D. N."
 | Up a level |
Group by: Item Type | No Grouping
Number of items: 1.
(2026) Analysis of whole-exome sequencing data from nearly 10,000 Iranian individuals: identification of recessive mitochondrial disease variants and proposal of a population-specific carrier screening panel. Human genomics. ISSN 1479-7364 (Electronic) 1473-9542 (Linking)