Genetic model of UBA5 deficiency highlights the involvement of both peripheral and central nervous systems and identifies widespread mitochondrial abnormalities

Rita J. Serrano, Viola Oorschot, Dashika Palipana, Vanessa Calcinotto, Carmen Sonntag, Georg Ramm, Robert J. Bryson-Richardson

Research output: Contribution to journal › Article › Research › peer-review

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Identifying disease genes for neurogenetic disorders using next generation sequencing
Laing, N. (Primary Chief Investigator (PCI)), Clarke, N. (Chief Investigator (CI)), MacArthur, D. (Chief Investigator (CI)), Nowak, K. J. (Chief Investigator (CI)), Ravenscroft, G. (Chief Investigator (CI)), Allcock, R. (Chief Investigator (CI)) & Bryson-Richardson, R. (Chief Investigator (CI))
National Health and Medical Research Council (NHMRC) (Australia)
1/01/15 → 31/12/19
Project: Research