Search Results - "Strbenac, D."

Generation of the iPSC line FINi002-A from a male Parkinson's disease patient carrying compound heterozygous mutations in the PRKN gene by Pavan, C., Jin, J., Jong, S., Strbenac, D., Davis, R.L., Sue, C.M., Johnston, J., Lynch, T., Halliday, G., Kirik, D., Parish, C.L., Thompson, L.H., Ovchinnikov, D.A.

“…The most common cause of autosomal recessive familial Parkinson’s disease (PD) are mutations in the PRKN/PARK2 gene encoding an E3 ubiquitin protein-ligase…”
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Savant Genome Browser 2: visualization and analysis for population-scale genomics by Fiume, Marc, Smith, Eric J M, Brook, Andrew, Strbenac, Dario, Turner, Brian, Mezlini, Aziz M, Robinson, Mark D, Wodak, Shoshana J, Brudno, Michael

“…High-throughput sequencing (HTS) technologies are providing an unprecedented capacity for data generation, and there is a corresponding need for efficient data…”
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