Analysis of DNA methylation associates the cystine–glutamate antiporter SLC7A11 with risk of Parkinson’s disease
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Published in Nature communications (06.03.2020)
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Evidence of a Recessively Inherited CCN3 Mutation as a Rare Cause of Early-Onset Parkinsonism
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Published in Frontiers in neurology (15.05.2020)
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Hunting for Familial Parkinson's Disease Mutations in the Post Genome Era
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Published in Genes (17.03.2021)
Published in Genes (17.03.2021)
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Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders
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Published in Genome Biology (26.03.2021)
Published in Genome Biology (26.03.2021)
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Pipeline to gene discovery - Analysing familial Parkinsonism in the Queensland Parkinson's Project
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Published in Parkinsonism & related disorders (01.04.2018)
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Rare POLG1 CAG variants do not influence Parkinson's disease or polymerase gamma function
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Published in Mitochondrion (01.03.2014)
Published in Mitochondrion (01.03.2014)
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ASYNCHRONOUS DIGITAL THRESHOLD DETECTOR FOR A DIGITAL DATA STORAGE CHANNEL
SUTARDJA, PANTAS, HUTCHINS, ROBERT ALLEN, MELAS, CONSTANTIN MICHAEL, BENTLEY, STEVEN R
Year of Publication 15.12.1998
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Year of Publication 15.12.1998
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Post-decoding error check with diagnostics for product codes
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Year of Publication 21.05.2019
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Year of Publication 21.05.2019
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