Publications
Export 1 results:
Author Title [ Year
] Filters: Author is Alodaib, Ahmad and Keyword is High-Throughput Nucleotide Sequencing [Clear All Filters]
Whole-exome sequencing identifies novel variants in PNPT1 causing oxidative phosphorylation defects and severe multisystem disease. Eur J Hum Genet 25, 79-84 (2016).
