Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction

Richard G. Lee, Maryam Sedghi, Mehri Salari, Anne-Marie J. Shearwood, Maike Stentenbach, Ariana Kariminejad, Hayley Goullee, Oliver Rackham, Nigel G. Laing, Homa Tajsharghi, Aleksandra Filipovska

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

27 Citations (Scopus)

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Finished

Improving outcomes for individuals and families affected by genetic disease
Laing, N. (Investigator 01)
NHMRC National Health and Medical Research Council
1/01/17 → 31/12/21
Project: Research
Neuromics: Application of Next Generation Sequencing to Neurogenetic Disorders in Australia
Laing, N. (Investigator 01)
NHMRC National Health and Medical Research Council
1/01/13 → 31/12/17
Project: Research
Mictchondrial Ribosomal Pentatricopeptide Domain Proteins Regulate Protein Synthesis in Health & Disease
Rackham, O. (Investigator 01), Filipovska, A. (Investigator 02), Small, I. (Investigator 03) & Whelan, J. (Investigator 04)
NHMRC National Health and Medical Research Council
1/01/11 → 31/12/13
Project: Research